Variant report

Variant	rs79654623
Chromosome Location	chr7:100424231-100424232
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	MAX	chr7:100422794-100425971	K562	blood:	n/a	chr7:100424953-100424963 chr7:100424987-100424997
2	MAX	chr7:100422691-100425951	MCF-7	breast:	n/a	chr7:100424953-100424963 chr7:100424987-100424997
3	ZBTB7A	chr7:100424207-100424813	ECC-1	luminal epithelium:	n/a	chr7:100424685-100424699 chr7:100424691-100424699
4	TEAD4	chr7:100423088-100424235	K562	blood:	n/a	n/a
5	RAD21	chr7:100422224-100424797	SK-N-SH	brain:	n/a	chr7:100423965-100423978
6	SIN3A	chr7:100423620-100425862	H1-hESC	embryonic stem cell:	n/a	chr7:100424058-100424069 chr7:100425437-100425450
7	MYC	chr7:100424213-100424272	HUVEC	blood vessel:	n/a	n/a
8	TAF1	chr7:100424198-100424672	H1-hESC	embryonic stem cell:	n/a	n/a
9	JUN	chr7:100422826-100426015	K562	blood:	n/a	n/a
10	MXI1	chr7:100422162-100426238	IMR90	lung:	n/a	n/a
11	SIN3AK20	chr7:100423958-100424539	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:100424160-100424310	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr7:100422524-100425952	SK-N-SH	brain:	n/a	chr7:100425569-100425590 chr7:100424947-100424956 chr7:100424800-100424813 chr7:100425592-100425613 chr7:100425599-100425612 chr7:100425602-100425610 chr7:100424039-100424052 chr7:100425597-100425615
14	TCF12	chr7:100423609-100424351	A549	lung:	n/a	n/a
15	CTCF	chr7:100424220-100424370	BJ	skin:	n/a	n/a
16	NFIC	chr7:100424027-100424243	HepG2	liver:	n/a	n/a
17	HA-E2F1	chr7:100424189-100425867	MCF-7	breast:	n/a	chr7:100424277-100424286 chr7:100425038-100425047
18	POLR2A	chr7:100423565-100425956	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr7:100422235-100427552	HUVEC	blood vessel:	n/a	n/a
20	SIN3AK20	chr7:100422470-100426001	MCF-7	breast:	n/a	n/a
21	NR2F2	chr7:100423113-100424459	K562	blood:	n/a	n/a
22	HDAC2	chr7:100424150-100425927	MCF-7	breast:	n/a	chr7:100424294-100424308 chr7:100424299-100424313 chr7:100425633-100425647
23	POLR2A	chr7:100423682-100427339	K562	blood:	n/a	n/a
24	SMC3	chr7:100422082-100425966	SK-N-SH	brain:	n/a	chr7:100425461-100425475 chr7:100425599-100425613 chr7:100423470-100423478 chr7:100423840-100423848 chr7:100423796-100423804
25	CTCF	chr7:100423377-100424830	A549	lung:	n/a	chr7:100424800-100424813 chr7:100424039-100424052
26	ZBTB7A	chr7:100423662-100424254	K562	blood:	n/a	n/a
27	POLR2A	chr7:100422030-100424812	SK-N-MC	brain:	n/a	n/a
28	MAZ	chr7:100422949-100425857	IMR90	lung:	n/a	chr7:100424953-100424963 chr7:100424987-100424997
29	UBTF	chr7:100423084-100425834	K562	blood:	n/a	n/a
30	SIN3AK20	chr7:100424193-100425907	PANC-1	pancreas:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100422826..100425783-chr7:100447402..100452140,5	K562	blood:
2	chr7:100026299..100028984-chr7:100423719..100425446,2	MCF-7	breast:
3	chr7:100303807..100306073-chr7:100423703..100425515,2	MCF-7	breast:
4	chr7:100423752..100426266-chr7:100463292..100466439,3	MCF-7	breast:
5	chr7:100302193..100303928-chr7:100423782..100426431,2	K562	blood:
6	chr7:100422507..100426422-chr7:100448675..100454510,8	MCF-7	breast:
7	chr7:100421802..100424702-chr7:100482689..100484467,2	MCF-7	breast:
8	chr7:100423550..100425060-chr7:100485976..100488045,2	K562	blood:
9	chr7:100422507..100425208-chr7:100700393..100702455,2	MCF-7	breast:
10	chr7:100317495..100321039-chr7:100423744..100425687,3	MCF-7	breast:
11	chr7:100026028..100027729-chr7:100422435..100425262,2	MCF-7	breast:
12	chr7:100422126..100425537-chr7:100471170..100475559,4	MCF-7	breast:
13	chr7:100317734..100318502-chr7:100423320..100424248,2	MCF-7	breast:
14	chr7:100223251..100225945-chr7:100423491..100425881,2	MCF-7	breast:
15	chr7:100410343..100413835-chr7:100422249..100426210,7	MCF-7	breast:
16	chr7:100423424..100426106-chr7:100484562..100490364,9	MCF-7	breast:
17	chr7:100396723..100397558-chr7:100423449..100424411,5	MCF-7	breast:
18	chr7:100208147..100211165-chr7:100422696..100426389,3	MCF-7	breast:
19	chr7:100301669..100305063-chr7:100423516..100428632,6	MCF-7	breast:
20	chr7:100423433..100426983-chr7:100448013..100452140,5	K562	blood:
21	chr20:49345925..49349495-chr7:100424000..100426504,3	MCF-7	breast:

Variant related genes	Relation type
EPHB4	TF binding region
SLC12A9	TF binding region
ENSG00000146834	Chromatin interaction
ENSG00000106327	Chromatin interaction
ENSG00000236305	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000106330	Chromatin interaction
ENSG00000130427	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000087087	Chromatin interaction
ENSG00000087077	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000222636	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000078487	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv470381	chr7:100240191-100431980	Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS 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	92 gene(s)	inside rSNPs	diseases
4	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription 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 miRNA target site	96 gene(s)	inside rSNPs	diseases
7	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
9	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription 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	92 gene(s)	inside rSNPs	diseases
10	nsv888797	chr7:100386900-100482026	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
11	nsv888798	chr7:100406144-100472826	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS 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 miRNA target site	71 gene(s)	inside rSNPs	diseases
12	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
13	nsv888800	chr7:100411278-100436446	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
15	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
16	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS 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 miRNA target site	90 gene(s)	inside rSNPs	diseases
17	esv3441371	chr7:100423841-100426389	Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100421800-100425000	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr7:100422200-100424600	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
3	chr7:100422200-100426400	Active TSS	Right Ventricle	heart
4	chr7:100422400-100424400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr7:100422400-100424400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
6	chr7:100422400-100424400	Flanking Active TSS	Fetal Muscle Leg	muscle
7	chr7:100422400-100425600	Active TSS	Lung	lung
8	chr7:100422400-100425800	Active TSS	Left Ventricle	heart
9	chr7:100422400-100426400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:100422400-100426400	Active TSS	Right Atrium	heart
11	chr7:100422600-100424400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:100422600-100424400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:100422600-100424400	Flanking Active TSS	Brain Germinal Matrix	brain
14	chr7:100422600-100424800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr7:100422600-100426400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:100422800-100424400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr7:100422800-100424400	Flanking Active TSS	Liver	Liver
18	chr7:100422800-100424600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
19	chr7:100422800-100424600	Flanking Active TSS	Fetal Muscle Trunk	muscle
20	chr7:100422800-100426400	Active TSS	Fetal Kidney	kidney
21	chr7:100422800-100427200	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr7:100423000-100424400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:100423000-100424400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:100423000-100424400	Flanking Active TSS	Osteobl	bone
25	chr7:100423000-100424600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr7:100423000-100424600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr7:100423000-100425400	Active TSS	Small Intestine	intestine
28	chr7:100423000-100425400	Active TSS	HMEC	breast
29	chr7:100423000-100426200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:100423000-100426600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:100423200-100424400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:100423200-100424600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr7:100423200-100425400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:100423200-100425800	Active TSS	Brain Anterior Caudate	brain
35	chr7:100423200-100425800	Active TSS	Fetal Lung	lung
36	chr7:100423400-100424400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
37	chr7:100423400-100424400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
38	chr7:100423400-100424400	Flanking Active TSS	HSMMtube	muscle
39	chr7:100423400-100424600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:100423400-100424600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr7:100423400-100425400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
42	chr7:100423400-100425400	Active TSS	Esophagus	oesophagus
43	chr7:100423400-100425400	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
44	chr7:100423400-100426000	Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr7:100423400-100426400	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr7:100423400-100426800	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr7:100423400-100427000	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr7:100423400-100427200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:100423600-100424600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:100423600-100425400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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