Variant report

Variant	rs565340522
Chromosome Location	chr1:180197894-180197895
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	ESR1	chr1:180197525-180198077	T-47D	breast:	n/a	chr1:180197837-180197854 chr1:180197836-180197853
2	CTBP2	chr1:180197846-180199045	H1-hESC	embryonic stem cell:	n/a	n/a
3	E2F6	chr1:180197561-180199243	H1-hESC	embryonic stem cell:	n/a	chr1:180199215-180199225 chr1:180198561-180198571 chr1:180199214-180199223
4	MAX	chr1:180197799-180199538	ECC-1	luminal epithelium:	n/a	chr1:180199482-180199492
5	E2F6	chr1:180197892-180199368	K562	blood:	n/a	chr1:180199215-180199225 chr1:180198561-180198571 chr1:180199214-180199223
6	MAX	chr1:180197823-180198552	MCF-7	breast:	n/a	n/a
7	ESR1	chr1:180197580-180197982	T-47D	breast:	n/a	chr1:180197837-180197854 chr1:180197836-180197853
8	SUZ12	chr1:180197213-180199016	NT2-D1	testis:	n/a	n/a
9	TCF7L2	chr1:180197701-180197900	Hela-S3	cervix:	n/a	n/a
10	ESR1	chr1:180197527-180198062	T-47D	breast:	n/a	chr1:180197837-180197854 chr1:180197836-180197853
11	ESR1	chr1:180197586-180198045	T-47D	breast:	n/a	chr1:180197837-180197854 chr1:180197836-180197853
12	HA-E2F1	chr1:180197498-180198973	MCF-7	breast:	n/a	chr1:180198561-180198571
13	MAX	chr1:180197655-180199566	H1-hESC	embryonic stem cell:	n/a	chr1:180199482-180199492
14	E2F6	chr1:180197762-180199140	H1-hESC	embryonic stem cell:	n/a	chr1:180198561-180198571
15	MAX	chr1:180197788-180198539	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAX	chr1:180197703-180201188	A549	lung:	n/a	chr1:180199482-180199492 chr1:180200203-180200213 chr1:180200952-180200961
17	FOXA1	chr1:180197589-180197924	T-47D	breast:	n/a	n/a
18	POLR2A	chr1:180197861-180199027	H1-neurons	neurons:	n/a	n/a
19	MAX	chr1:180197791-180199659	A549	lung:	n/a	chr1:180199482-180199492
20	FOXA1	chr1:180197542-180197976	T-47D	breast:	n/a	n/a
21	MAX	chr1:180197826-180199410	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F6	chr1:180197777-180199261	A549	lung:	n/a	chr1:180199215-180199225 chr1:180198561-180198571 chr1:180199214-180199223
23	POLR2A	chr1:180196969-180199142	H1-neurons	neurons:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:180197504..180199167-chr1:180224925..180226535,2	MCF-7	breast:
2	chr1:179832613..179834557-chr1:180196646..180198975,2	MCF-7	breast:
3	chr1:180177496..180179586-chr1:180196486..180198566,3	K562	blood:
4	chr1:180136376..180137428-chr1:180197371..180198301,4	MCF-7	breast:
5	chr1:180197757..180200322-chr1:180217302..180220148,2	K562	blood:
6	chr1:180136376..180137616-chr1:180197323..180198301,4	MCF-7	breast:
7	chr1:180157764..180160729-chr1:180196773..180199044,2	MCF-7	breast:
8	chr1:180197528..180200245-chr1:180468948..180472883,3	MCF-7	breast:
9	chr1:180196398..180198939-chr20:52539225..52540761,2	MCF-7	breast:
10	chr1:180179631..180182619-chr1:180197309..180199073,2	K562	blood:
11	chr1:179843890..179844531-chr1:180197550..180198249,2	MCF-7	breast:
12	chr1:180143261..180143849-chr1:180197310..180198264,2	MCF-7	breast:
13	chr1:180183289..180186252-chr1:180197125..180198628,2	MCF-7	breast:

Variant related genes	Relation type
LHX4	TF binding region
ENSG00000121454	Chromatin interaction
ENSG00000135847	Chromatin interaction
ENSG00000258664	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429936	chr1:179790343-180214343	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1003739	chr1:180027760-180483292	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv535217	chr1:180027760-180483292	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv1012558	chr1:180027960-180217613	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv535218	chr1:180027960-180217613	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv497930	chr1:180031321-180220723	Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv533073	chr1:180031328-180217612	Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription 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 target site	33 gene(s)	inside rSNPs	diseases
8	nsv916937	chr1:180031328-180220685	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv1007590	chr1:180121480-180236452	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
10	nsv999104	chr1:180121480-180242659	Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1002133	chr1:180127036-180230081	Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv1011134	chr1:180127616-180201104	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv999182	chr1:180127616-180236452	Genic enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	nsv1005512	chr1:180127616-180242659	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv832004	chr1:180128502-180335540	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
16	nsv1012816	chr1:180132688-180201104	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
17	nsv1012145	chr1:180132688-180236452	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv466239	chr1:180145978-180268476	Bivalent Enhancer ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
19	nsv548345	chr1:180145978-180268476	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
20	nsv1005793	chr1:180150400-180205202	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
21	nsv1005073	chr1:180152550-180250783	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
22	nsv535219	chr1:180152550-180250783	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
23	nsv1001477	chr1:180172903-180298287	Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv535220	chr1:180172903-180298287	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
25	nsv498075	chr1:180179441-180278544	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
26	nsv872575	chr1:180186713-180238243	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
27	esv3361812	chr1:180197754-180200702	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180197400-180201000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr1:180197600-180198000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
3	chr1:180197600-180198000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
4	chr1:180197600-180198000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
5	chr1:180197600-180198000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr1:180197600-180198200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
7	chr1:180197600-180201000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
8	chr1:180197800-180198000	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:180197800-180198000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:180197800-180198000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
11	chr1:180197800-180198000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
12	chr1:180197800-180198000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:180197800-180198000	Bivalent Enhancer	Fetal Brain Female	brain
14	chr1:180197800-180198000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
15	chr1:180197800-180198000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
16	chr1:180197800-180198200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:180197800-180198200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr1:180197800-180198200	Bivalent Enhancer	Primary B cells from cord blood	blood
19	chr1:180197800-180198200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
20	chr1:180197800-180198200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
21	chr1:180197800-180198200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:180197800-180198200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:180197800-180198200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:180197800-180198200	Bivalent Enhancer	Brain Germinal Matrix	brain
25	chr1:180197800-180198200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:180197800-180198200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr1:180197800-180198200	Enhancers	Gastric	stomach
28	chr1:180197800-180198200	ZNF genes & repeats	Right Atrium	heart
29	chr1:180197800-180198200	Bivalent/Poised TSS	Right Ventricle	heart
30	chr1:180197800-180198200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
31	chr1:180197800-180198400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr1:180197800-180198400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:180197800-180198400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
34	chr1:180197800-180198400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:180197800-180198400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
36	chr1:180197800-180198400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:180197800-180198400	Bivalent Enhancer	Esophagus	oesophagus
38	chr1:180197800-180198400	Bivalent Enhancer	Fetal Stomach	stomach
39	chr1:180197800-180198400	Enhancers	Pancreas	Pancrea
40	chr1:180197800-180198600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:180197800-180198800	Bivalent Enhancer	Fetal Brain Male	brain
42	chr1:180197800-180201000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
43	chr1:180197800-180201000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
44	chr1:180197800-180201000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
45	chr1:180197800-180201200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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