Variant report

Variant	rs555410739
Chromosome Location	chr14:21732033-21732034
allele	-/TGT
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	POLR2A	chr14:21728426-21734336	GM12891	blood:	n/a	n/a
2	STAT5A	chr14:21731708-21733230	GM12878	blood:	n/a	chr14:21732454-21732463 chr14:21732453-21732462 chr14:21731920-21731932
3	POLR2A	chr14:21728614-21735024	GM12878	blood:	n/a	n/a
4	POLR2A	chr14:21731418-21732316	PFSK-1	brain:	n/a	n/a
5	POLR2A	chr14:21731482-21732593	GM12891	blood:	n/a	n/a
6	POLR2A	chr14:21731777-21732568	Hela-S3	cervix:	n/a	n/a
7	STAT3	chr14:21731940-21732873	MCF10A-Er-Src	breast:	n/a	chr14:21732454-21732463 chr14:21732453-21732462
8	NFIC	chr14:21731907-21732768	GM12878	blood:	n/a	n/a
9	MXI1	chr14:21731595-21732787	GM12878	blood:	n/a	n/a
10	BATF	chr14:21731822-21732559	GM12878	blood:	n/a	chr14:21732455-21732465 chr14:21732451-21732461
11	FOXM1	chr14:21731728-21732516	GM12878	blood:	n/a	chr14:21732008-21732016
12	POLR2A	chr14:21731506-21732242	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr14:21731403-21733378	GM12892	blood:	n/a	n/a
14	POLR2A	chr14:21728611-21734968	GM12878	blood:	n/a	n/a
15	POLR2A	chr14:21731492-21732422	PANC-1	pancreas:	n/a	n/a
16	POLR2A	chr14:21731901-21732698	SK-N-SH	brain:	n/a	n/a
17	POLR2A	chr14:21731953-21732154	SK-N-SH	brain:	n/a	n/a
18	POLR2A	chr14:21731735-21732041	K562	blood:	n/a	n/a
19	POLR2A	chr14:21731474-21733227	IMR90	lung:	n/a	n/a
20	FOS	chr14:21731786-21732880	MCF10A-Er-Src	breast:	n/a	chr14:21732007-21732018 chr14:21732454-21732461 chr14:21732454-21732463 chr14:21732452-21732463 chr14:21732453-21732463 chr14:21732009-21732021 chr14:21732454-21732462 chr14:21732453-21732462
21	POLR2A	chr14:21731874-21732120	GM12878	blood:	n/a	n/a
22	POLR2A	chr14:21731625-21732545	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr14:21731499-21733364	SK-N-MC	brain:	n/a	n/a
24	ATF2	chr14:21731544-21732278	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr14:21731395-21732632	GM12891	blood:	n/a	n/a
26	POLR2A	chr14:21731447-21732543	Hela-S3	cervix:	n/a	n/a
27	WRNIP1	chr14:21731879-21732190	GM12878	blood:	n/a	n/a
28	POLR2A	chr14:21728514-21734782	HepG2	liver:	n/a	n/a
29	POLR2A	chr14:21731778-21734317	K562	blood:	n/a	n/a
30	CHD1	chr14:21730830-21732887	GM12878	blood:	n/a	n/a
31	CHD1	chr14:21731403-21732196	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr14:21731435-21733211	HepG2	liver:	n/a	n/a
33	POLR2A	chr14:21728424-21734236	HepG2	liver:	n/a	n/a
34	POLR2A	chr14:21731378-21738564	GM12878	blood:	n/a	n/a
35	POLR2A	chr14:21731441-21732617	K562	blood:	n/a	n/a
36	POLR2A	chr14:21728578-21737722	K562	blood:	n/a	n/a
37	HEY1	chr14:21731491-21732571	HepG2	liver:	n/a	n/a
38	NFATC1	chr14:21731767-21734347	GM12878	blood:	n/a	n/a
39	FOSL2	chr14:21731937-21732636	A549	lung:	n/a	chr14:21732007-21732018 chr14:21732454-21732461 chr14:21732454-21732463 chr14:21732453-21732463 chr14:21732009-21732021 chr14:21732454-21732462 chr14:21732453-21732462
40	POLR2A	chr14:21731732-21732305	K562	blood:	n/a	n/a
41	POLR2A	chr14:21731417-21732579	GM12892	blood:	n/a	n/a
42	JUND	chr14:21731389-21733205	SK-N-SH	brain:	n/a	chr14:21732007-21732018 chr14:21732454-21732461 chr14:21732452-21732463 chr14:21732454-21732463 chr14:21732453-21732463 chr14:21732009-21732021 chr14:21732454-21732462 chr14:21732453-21732462
43	POLR2A	chr14:21731935-21732148	GM12878	blood:	n/a	n/a
44	POLR2A	chr14:21731438-21732574	GM12892	blood:	n/a	n/a
45	HEY1	chr14:21731815-21732404	K562	blood:	n/a	n/a
46	POLR2A	chr14:21731837-21732171	HL-60	blood:	n/a	n/a
47	POLR2A	chr14:21731492-21733388	GM12891	blood:	n/a	n/a
48	NFATC1	chr14:21731782-21733274	GM12878	blood:	n/a	n/a
49	MTA3	chr14:21731884-21732725	GM12878	blood:	n/a	n/a
50	POLR2A	chr14:21731404-21735357	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21729912..21732388-chr14:21794121..21797950,3	K562	blood:
2	chr14:21731892..21738562-chr14:21850801..21854193,10	MCF-7	breast:
3	chr14:21730988..21732970-chr14:21824045..21825778,2	K562	blood:
4	chr14:21731325..21733922-chr14:21791322..21794128,2	MCF-7	breast:
5	chr14:21731095..21732813-chr14:21767081..21768936,2	K562	blood:
6	chr14:21731127..21734828-chr14:21850549..21852828,3	K562	blood:
7	chr14:21730203..21732388-chr14:21795365..21797950,2	K562	blood:
8	chr14:21731613..21734582-chr14:21826282..21828114,3	MCF-7	breast:

Variant related genes	Relation type
HNRNPC	TF binding region
ENSG00000260830	Chromatin interaction
ENSG00000092201	Chromatin interaction
ENSG00000092200	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking 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	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS 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 target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking 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	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1048032	chr14:21602341-21847247	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	nsv541978	chr14:21602341-21847247	Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv901477	chr14:21625262-21750308	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	nsv901478	chr14:21626497-21750308	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv1044822	chr14:21659344-21860081	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv541979	chr14:21672540-21735893	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
16	nsv541980	chr14:21672540-21742729	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
17	nsv541982	chr14:21676221-21735893	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
18	nsv541983	chr14:21676221-21742729	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
19	esv1825348	chr14:21691941-21829404	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
20	nsv1051407	chr14:21692670-21907366	Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
21	nsv541984	chr14:21692670-21907366	Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Enhancers Bivalent Enhancer 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 target site	37 gene(s)	inside rSNPs	diseases
22	nsv530010	chr14:21692670-21923767	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
23	nsv541986	chr14:21692703-21735893	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
24	nsv541987	chr14:21692703-21742729	Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
25	nsv541988	chr14:21696056-21735893	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
26	nsv541989	chr14:21696056-21742729	Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
27	esv3357025	chr14:21702262-21737534	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
28	nsv541990	chr14:21702771-21757737	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
29	nsv428617	chr14:21721165-21871164	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
30	nsv983804	chr14:21730434-21759672	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21702200-21735600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:21720400-21733600	Genic enhancers	Primary T cells fromperipheralblood	blood
3	chr14:21723800-21733000	Strong transcription	Fetal Muscle Leg	muscle
4	chr14:21723800-21734200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:21724000-21733800	Strong transcription	Fetal Stomach	stomach
6	chr14:21724200-21735600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:21726000-21733000	Strong transcription	Fetal Muscle Trunk	muscle
8	chr14:21726200-21733600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
9	chr14:21726800-21733400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr14:21728600-21737400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
11	chr14:21728800-21733800	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr14:21729200-21733200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
13	chr14:21729200-21735600	Genic enhancers	Primary B cells from peripheral blood	blood
14	chr14:21729200-21736800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
15	chr14:21729600-21732800	Genic enhancers	Brain Germinal Matrix	brain
16	chr14:21729600-21733800	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr14:21729600-21734200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:21729600-21734800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:21729800-21733600	Genic enhancers	Fetal Brain Female	brain
20	chr14:21729800-21735400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
21	chr14:21730000-21732800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
22	chr14:21730000-21733600	Genic enhancers	Liver	Liver
23	chr14:21730000-21733600	Genic enhancers	Rectal Mucosa Donor 29	rectum
24	chr14:21730000-21733800	Genic enhancers	Brain Hippocampus Middle	brain
25	chr14:21730000-21734000	Genic enhancers	Brain Cingulate Gyrus	brain
26	chr14:21730000-21734000	Strong transcription	Placenta Amnion	Placenta Amnion
27	chr14:21730000-21734200	Genic enhancers	Brain Inferior Temporal Lobe	brain
28	chr14:21730000-21734200	Genic enhancers	Rectal Mucosa Donor 31	rectum
29	chr14:21730200-21737600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
30	chr14:21730400-21735000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr14:21730600-21733200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr14:21730600-21734200	Genic enhancers	Left Ventricle	heart
33	chr14:21730600-21734200	Enhancers	Small Intestine	intestine
34	chr14:21730600-21734600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr14:21730600-21734600	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
36	chr14:21730600-21734600	Genic enhancers	Fetal Lung	lung
37	chr14:21730600-21734800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr14:21730600-21735400	Genic enhancers	Primary monocytes fromperipheralblood	blood
39	chr14:21730600-21735400	Genic enhancers	Primary B cells from cord blood	blood
40	chr14:21730600-21736200	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr14:21730800-21732200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:21730800-21732200	Transcr. at gene 5' and 3'	Hela-S3	cervix
43	chr14:21730800-21736400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:21730800-21736800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:21731000-21732800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:21731000-21732800	Strong transcription	Placenta	Placenta
47	chr14:21731000-21732800	Weak transcription	Lung	lung
48	chr14:21731000-21732800	Weak transcription	Pancreas	Pancrea
49	chr14:21731000-21733000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:21731000-21733000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links