Variant report

Variant	rs544979009
Chromosome Location	chr2:111877800-111877801
allele	A/G
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	E2F6	chr2:111877408-111879340	K562	blood:	n/a	chr2:111878414-111878423 chr2:111877747-111877759 chr2:111877478-111877490 chr2:111878679-111878691 chr2:111877963-111877973 chr2:111878285-111878294 chr2:111878171-111878181
2	MYBL2	chr2:111877719-111878714	HepG2	liver:	n/a	n/a
3	ELK1	chr2:111877644-111877994	GM12878	blood:	n/a	n/a
4	MAX	chr2:111877563-111881015	NB4	blood:	n/a	chr2:111878235-111878244 chr2:111878233-111878243 chr2:111878683-111878693 chr2:111879218-111879227
5	MAX	chr2:111877317-111879304	H1-hESC	embryonic stem cell:	n/a	chr2:111878235-111878244 chr2:111878233-111878243 chr2:111878683-111878693 chr2:111877479-111877489 chr2:111879218-111879227
6	E2F6	chr2:111876311-111880584	H1-hESC	embryonic stem cell:	n/a	chr2:111876443-111876455 chr2:111878414-111878423 chr2:111880549-111880558 chr2:111880095-111880104 chr2:111877747-111877759 chr2:111877347-111877357 chr2:111876622-111876632 chr2:111877478-111877490 chr2:111878679-111878691 chr2:111877963-111877973 chr2:111880318-111880330 chr2:111878285-111878294 chr2:111878171-111878181 chr2:111880053-111880060
7	POLR2A	chr2:111877782-111879129	MCF-7	breast:	n/a	n/a
8	TCF12	chr2:111877680-111880212	A549	lung:	n/a	n/a
9	SIN3AK20	chr2:111877611-111881217	MCF-7	breast:	n/a	n/a
10	TCF12	chr2:111877517-111879634	ECC-1	luminal epithelium:	n/a	n/a
11	EBF1	chr2:111877547-111877924	GM12878	blood:	n/a	n/a
12	NR2F2	chr2:111877591-111878775	MCF-7	breast:	n/a	n/a
13	E2F6	chr2:111877661-111877922	K562	blood:	n/a	chr2:111877747-111877759
14	POLR2A	chr2:111877738-111878830	K562	blood:	n/a	n/a
15	SUZ12	chr2:111874709-111878454	NT2-D1	testis:	n/a	n/a
16	STAT1	chr2:111877756-111878558	GM12878	blood:	n/a	n/a
17	MAX	chr2:111877542-111881163	HepG2	liver:	n/a	chr2:111878235-111878244 chr2:111878233-111878243 chr2:111878683-111878693 chr2:111879218-111879227
18	POLR2A	chr2:111877432-111881054	K562	blood:	n/a	n/a
19	HDAC2	chr2:111877619-111878541	HepG2	liver:	n/a	chr2:111877674-111877688 chr2:111877675-111877689
20	GATA3	chr2:111877704-111879021	A549	lung:	n/a	n/a
21	MAX	chr2:111877713-111879368	A549	lung:	n/a	chr2:111878235-111878244 chr2:111878233-111878243 chr2:111878683-111878693 chr2:111879218-111879227
22	SMARCB1	chr2:111877080-111881031	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr2:111877652-111881216	H1-hESC	embryonic stem cell:	n/a	n/a
24	E2F6	chr2:111877723-111880882	Hela-S3	cervix:	n/a	chr2:111878414-111878423 chr2:111880549-111880558 chr2:111880095-111880104 chr2:111877747-111877759 chr2:111878679-111878691 chr2:111877963-111877973 chr2:111880318-111880330 chr2:111878285-111878294 chr2:111878171-111878181 chr2:111880053-111880060
25	POLR2A	chr2:111877744-111880423	NB4	blood:	n/a	n/a
26	MYC	chr2:111877505-111879474	K562	blood:	n/a	chr2:111878235-111878244 chr2:111878233-111878243 chr2:111878683-111878693 chr2:111879218-111879227
27	TBP	chr2:111877793-111879385	K562	blood:	n/a	n/a
28	MAZ	chr2:111877230-111879730	GM12878	blood:	n/a	chr2:111878235-111878244 chr2:111878683-111878693 chr2:111877479-111877489 chr2:111879218-111879227
29	YY1	chr2:111877574-111878752	HepG2	liver:	n/a	chr2:111878164-111878173 chr2:111878499-111878510 chr2:111878164-111878175 chr2:111878165-111878179 chr2:111878414-111878423 chr2:111878039-111878050 chr2:111878168-111878182 chr2:111878285-111878299 chr2:111878170-111878179 chr2:111878159-111878173 chr2:111878164-111878178
30	SUZ12	chr2:111875129-111878150	H1-hESC	embryonic stem cell:	n/a	n/a
31	UBTF	chr2:111877688-111881146	K562	blood:	n/a	n/a
32	CHD2	chr2:111877705-111879159	Hela-S3	cervix:	n/a	chr2:111878005-111878015 chr2:111878901-111878911
33	MXI1	chr2:111877406-111881885	SK-N-SH	brain:	n/a	n/a
34	YY1	chr2:111877707-111878744	K562	blood:	n/a	chr2:111878164-111878173 chr2:111878499-111878510 chr2:111878164-111878175 chr2:111878165-111878179 chr2:111878414-111878423 chr2:111878039-111878050 chr2:111878168-111878182 chr2:111878285-111878299 chr2:111878170-111878179 chr2:111878159-111878173 chr2:111878164-111878178
35	CHD2	chr2:111877596-111879005	GM12878	blood:	n/a	chr2:111878005-111878015 chr2:111878901-111878911
36	E2F6	chr2:111877377-111879315	H1-hESC	embryonic stem cell:	n/a	chr2:111878414-111878423 chr2:111877747-111877759 chr2:111877478-111877490 chr2:111878679-111878691 chr2:111877963-111877973 chr2:111878285-111878294 chr2:111878171-111878181
37	CBX3	chr2:111877569-111878634	K562	blood:	n/a	n/a
38	BHLHE40	chr2:111877526-111880906	K562	blood:	n/a	chr2:111878164-111878180 chr2:111878158-111878174 chr2:111879083-111879099 chr2:111878389-111878405 chr2:111880077-111880093 chr2:111878166-111878182 chr2:111879143-111879159
39	POLR2A	chr2:111877703-111879109	GM12892	blood:	n/a	n/a
40	CTBP2	chr2:111874524-111881050	H1-hESC	embryonic stem cell:	n/a	n/a
41	SPI1	chr2:111877637-111877828	GM12878	blood:	n/a	chr2:111877715-111877724
42	NR2F2	chr2:111877604-111878060	K562	blood:	n/a	n/a
43	BRCA1	chr2:111877770-111878768	Hela-S3	cervix:	n/a	chr2:111877909-111877918
44	ZBTB7A	chr2:111877698-111878536	K562	blood:	n/a	chr2:111878142-111878151
45	POLR2A	chr2:111877766-111881072	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr2:111877690-111879624	PANC-1	pancreas:	n/a	n/a
47	POLR2A	chr2:111877708-111878782	HepG2	liver:	n/a	n/a
48	SPI1	chr2:111877518-111877889	GM12878	blood:	n/a	chr2:111877715-111877724
49	POLR2A	chr2:111877725-111879356	GM15510	blood:	n/a	n/a
50	MAX	chr2:111877586-111880464	A549	lung:	n/a	chr2:111878235-111878244 chr2:111878233-111878243 chr2:111878683-111878693 chr2:111879218-111879227

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:111877753-111877803	HAEpiC	amniotic membrane:	n/a
2	chr2:111877753-111877803	RPTEC	kidney:	n/a
3	chr2:111877753-111877803	NHDF-neo	bronchial:	n/a
4	chr2:111877753-111877803	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:111877753-111877803	HRPEpiC	eye:	n/a
6	chr2:111877753-111877803	GM19239	blood:	n/a
7	chr2:111877753-111877803	HepG2	liver:	n/a
8	chr2:111877753-111877803	BE2_C	brain:	n/a
9	chr2:111877753-111877803	NHBE	bronchial:	n/a
10	chr2:111877753-111877803	Hela-S3	cervix:	n/a
11	chr2:111877753-111877803	Jurkat	blood:	n/a
12	chr2:111877753-111877803	NT2-D1	testis:	n/a
13	chr2:111877753-111877803	SK-N-SH	brain:	n/a
14	chr2:111877753-111877803	GM12878	blood:	n/a
15	chr2:111877753-111877803	Hepatocyte	liver:	n/a
16	chr2:111877753-111877803	HRCEpiC	kidney:	n/a
17	chr2:111877753-111877803	HCF	heart:	n/a
18	chr2:111877753-111877803	AG04449	skin:	fetal
19	chr2:111877753-111877803	HCPEpiC	choroid plexus:	n/a
20	chr2:111877753-111877803	U87	brain:	n/a
21	chr2:111877753-111877803	Caco-2	colon:	n/a
22	chr2:111877753-111877803	HRE	kidney:	n/a
23	chr2:111877753-111877803	PFSK-1	brain:	n/a
24	chr2:111877753-111877803	BJ	skin:	n/a
25	chr2:111877753-111877803	IMR90	lung:	fetal
26	chr2:111877753-111877803	AG09309	skin:	n/a
27	chr2:111877753-111877803	ProgFib	skin:	n/a
28	chr2:111877753-111877803	MCF10A-Er-Src	breast:	n/a
29	chr2:111877753-111877803	T-47D	breast:	n/a
30	chr2:111877753-111877803	HMEC	breast:	n/a
31	chr2:111877753-111877803	HL-60	blood:	n/a
32	chr2:111877753-111877803	AG09319	gingival:	n/a
33	chr2:111877753-111877803	AG10803	skin:	n/a
34	chr2:111877753-111877803	HCM	heart:	n/a
35	chr2:111877753-111877803	SK-N-SH_RA	brain:	n/a
36	chr2:111877753-111877803	GM12892	blood:	n/a
37	chr2:111877753-111877803	H1-hESC	embryonic stem cell:	embryo
38	chr2:111877753-111877803	AG04450	lung:	fetal
39	chr2:111877753-111877803	HUVEC	blood vessel:	n/a
40	chr2:111877753-111877803	A549	lung:	n/a
41	chr2:111877753-111877803	LNCaP	prostate:	n/a
42	chr2:111877753-111877803	HEEpiC	esophagus:	n/a
43	chr2:111877753-111877803	MCF-7	breast:	n/a
44	chr2:111877753-111877803	NH-A	brain:	n/a
45	chr2:111877753-111877803	PANC-1	pancreas:	n/a
46	chr2:111877753-111877803	HCT-116	colon:	n/a
47	chr2:111877753-111877803	SAEC	small airway:	n/a
48	chr2:111877753-111877803	GM06990	blood:	n/a
49	chr2:111877753-111877803	AoSMC	blood vessel:	n/a
50	chr2:111877753-111877803	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:111869458..111872537-chr2:111876483..111880583,5	MCF-7	breast:
2	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
3	chr2:111875880..111877905-chr2:111996338..111997967,2	K562	blood:
4	chr2:111876826..111879311-chr2:111966028..111968773,2	K562	blood:
5	chr12:28120103..28122878-chr2:111877498..111879183,2	MCF-7	breast:

Variant related genes	Relation type
BCL2L11	TF binding region
ENSG00000204581	TF binding region
BCL2L11	CpG island
ENSG00000204581	CpG island
ENSG00000204581	Chromatin interaction
ENSG00000087494	Chromatin interaction
ENSG00000172965	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv834331	chr2:111812139-112004678	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv874842	chr2:111870220-111892984	Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Enhancers 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	17 gene(s)	inside rSNPs	diseases
4	nsv829618	chr2:111875627-111881547	Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
5	esv3338590	chr2:111876081-111880479	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
6	esv3373707	chr2:111877306-111879854	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111874400-111877800	Enhancers	Spleen	Spleen
2	chr2:111874400-111878200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
3	chr2:111874400-111879800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr2:111874600-111878000	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
5	chr2:111874600-111878200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
6	chr2:111874600-111878200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
7	chr2:111874600-111878400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:111874800-111878000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
9	chr2:111874800-111878000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
10	chr2:111874800-111878000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
11	chr2:111874800-111878000	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr2:111874800-111878000	Flanking Bivalent TSS/Enh	Thymus	Thymus
13	chr2:111874800-111878200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
14	chr2:111874800-111878200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:111874800-111878200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:111874800-111878200	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr2:111874800-111878200	Flanking Active TSS	Right Ventricle	heart
18	chr2:111874800-111879600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:111874800-111880000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr2:111875000-111877800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
21	chr2:111875000-111878000	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
22	chr2:111875000-111878200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:111875200-111878200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr2:111875200-111878200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:111875200-111878200	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
26	chr2:111875200-111880000	Bivalent Enhancer	Fetal Brain Male	brain
27	chr2:111875400-111877800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
28	chr2:111875400-111878000	Weak transcription	Aorta	Aorta
29	chr2:111875400-111878000	Bivalent Enhancer	Fetal Lung	lung
30	chr2:111875600-111877800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr2:111875600-111877800	Weak transcription	Ovary	ovary
32	chr2:111875600-111877800	Weak transcription	HSMMtube	muscle
33	chr2:111875600-111878000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
34	chr2:111875600-111880000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
35	chr2:111875600-111881200	Active TSS	Psoas Muscle	Psoas
36	chr2:111876000-111877800	Flanking Bivalent TSS/Enh	Placenta	Placenta
37	chr2:111876000-111878000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
38	chr2:111876200-111877800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr2:111876200-111877800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
40	chr2:111876200-111878200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:111876200-111880000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr2:111876400-111877800	Enhancers	Lung	lung
43	chr2:111876400-111878400	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr2:111876400-111880000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
45	chr2:111876600-111878200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
46	chr2:111876800-111877800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:111876800-111877800	Enhancers	Gastric	stomach
48	chr2:111876800-111877800	Bivalent Enhancer	NH-A	brain
49	chr2:111876800-111878000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr2:111877000-111877800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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