Variant report

Variant	rs113417611
Chromosome Location	chr21:46494181-46494182
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:61)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	YY1	chr21:46493674-46494864	K562	blood:	n/a	chr21:46494208-46494222 chr21:46494833-46494847 chr21:46494211-46494220 chr21:46494263-46494274 chr21:46494205-46494219
2	POLR2A	chr21:46494032-46494410	U87	brain:	n/a	n/a
3	POLR2A	chr21:46494115-46494488	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr21:46493263-46495236	K562	blood:	n/a	n/a
5	BCLAF1	chr21:46493450-46494317	K562	blood:	n/a	chr21:46494282-46494295 chr21:46494207-46494220
6	BHLHE40	chr21:46494036-46494443	GM12878	blood:	n/a	n/a
7	RCOR1	chr21:46493310-46494408	K562	blood:	n/a	n/a
8	MYBL2	chr21:46493927-46494401	HepG2	liver:	n/a	n/a
9	POLR2A	chr21:46493501-46494497	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr21:46493074-46495782	MCF-7	breast:	n/a	n/a
11	ZC3H11A	chr21:46493426-46494398	K562	blood:	n/a	n/a
12	SP2	chr21:46494038-46494235	K562	blood:	n/a	n/a
13	BCL3	chr21:46493435-46495331	K562	blood:	n/a	chr21:46494282-46494295 chr21:46494993-46495006 chr21:46494353-46494366 chr21:46494989-46495002 chr21:46494938-46494951 chr21:46494830-46494839 chr21:46494988-46495001 chr21:46494207-46494220
14	CHD2	chr21:46493723-46494288	GM12878	blood:	n/a	n/a
15	THAP1	chr21:46493970-46494437	K562	blood:	n/a	n/a
16	POLR2A	chr21:46493412-46494434	PBDE	blood:	n/a	n/a
17	CEBPD	chr21:46493939-46494434	HepG2	liver:	n/a	n/a
18	CHD2	chr21:46493766-46494590	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr21:46493084-46495667	K562	blood:	n/a	n/a
20	CREB1	chr21:46493985-46494470	A549	lung:	n/a	n/a
21	PML	chr21:46493184-46494595	MCF-7	breast:	n/a	n/a
22	POLR2A	chr21:46493666-46494737	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr21:46493678-46494747	GM15510	blood:	n/a	n/a
24	POLR2A	chr21:46493543-46495715	Hela-S3	cervix:	n/a	n/a
25	BHLHE40	chr21:46493364-46494410	K562	blood:	n/a	chr21:46493432-46493448 chr21:46493397-46493413
26	MYC	chr21:46493950-46494424	K562	blood:	n/a	n/a
27	POLR2A	chr21:46493607-46495487	HEK293	kidney:	n/a	n/a
28	ZBTB7A	chr21:46493952-46494442	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr21:46493615-46495019	ProgFib	skin:	n/a	n/a
30	PBX3	chr21:46493673-46494588	A549	lung:	n/a	n/a
31	TAF7	chr21:46493625-46494412	K562	blood:	n/a	n/a
32	POLR2A	chr21:46493408-46495654	K562	blood:	n/a	n/a
33	POLR2A	chr21:46493601-46495258	HepG2	liver:	n/a	n/a
34	POLR2A	chr21:46492515-46494487	K562	blood:	n/a	n/a
35	POLR2A	chr21:46493379-46495527	K562	blood:	n/a	n/a
36	JUND	chr21:46493966-46494353	HepG2	liver:	n/a	chr21:46494207-46494216
37	YY1	chr21:46493616-46494430	K562	blood:	n/a	chr21:46494208-46494222 chr21:46494211-46494220 chr21:46494263-46494274 chr21:46494205-46494219
38	POLR2A	chr21:46493378-46494744	MCF10A-Er-Src	breast:	n/a	n/a
39	TCF12	chr21:46493958-46494424	HepG2	liver:	n/a	n/a
40	HEY1	chr21:46493480-46495777	K562	blood:	n/a	chr21:46494290-46494305 chr21:46494988-46495003 chr21:46494931-46494946 chr21:46494197-46494212 chr21:46495443-46495458 chr21:46494236-46494251 chr21:46494206-46494221
41	ZBTB7A	chr21:46493662-46494434	ECC-1	luminal epithelium:	n/a	n/a
42	FOXP2	chr21:46493962-46494499	PFSK-1	brain:	n/a	n/a
43	POLR2A	chr21:46493543-46494828	HCT-116	colon:	n/a	n/a
44	BCL11A	chr21:46493950-46494241	GM12878	blood:	n/a	chr21:46494207-46494220
45	SIN3AK20	chr21:46493002-46494465	MCF-7	breast:	n/a	n/a
46	POLR2A	chr21:46494117-46494510	GM12878	blood:	n/a	n/a
47	EP300	chr21:46493958-46494364	T-47D	breast:	n/a	chr21:46494208-46494217 chr21:46494211-46494220
48	CREB1	chr21:46493606-46494539	K562	blood:	n/a	n/a
49	POLR2A	chr21:46492353-46497285	IMR90	lung:	n/a	n/a
50	POLR2A	chr21:46494020-46494455	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:46494133-46494183	NHBE	bronchial:	n/a
2	chr21:46494133-46494183	ProgFib	skin:	n/a
3	chr21:46494133-46494183	CMK	blood:	n/a
4	chr21:46494133-46494183	AG04449	skin:	fetal
5	chr21:46494133-46494183	AG10803	skin:	n/a
6	chr21:46494133-46494183	GM12892	blood:	n/a
7	chr21:46494133-46494183	HRPEpiC	eye:	n/a
8	chr21:46494133-46494183	Jurkat	blood:	n/a
9	chr21:46494133-46494183	NHDF-neo	bronchial:	n/a
10	chr21:46494133-46494183	HRCEpiC	kidney:	n/a
11	chr21:46494133-46494183	LNCaP	prostate:	n/a
12	chr21:46494133-46494183	PANC-1	pancreas:	n/a
13	chr21:46494133-46494183	ovcar-3	ovarian:	n/a
14	chr21:46494133-46494183	HIPEpiC	eye:	n/a
15	chr21:46494133-46494183	NH-A	brain:	n/a
16	chr21:46494133-46494183	H1-hESC	embryonic stem cell:	embryo
17	chr21:46494133-46494183	AG09319	gingival:	n/a
18	chr21:46494133-46494183	HEK293	kidney:	embryo
19	chr21:46494133-46494183	ECC-1	luminal epithelium:	n/a
20	chr21:46494133-46494183	T-47D	breast:	n/a
21	chr21:46494133-46494183	IMR90	lung:	fetal
22	chr21:46494133-46494183	HCPEpiC	choroid plexus:	n/a
23	chr21:46494133-46494183	SK-N-SH	brain:	n/a
24	chr21:46494133-46494183	HepG2	liver:	n/a
25	chr21:46494133-46494183	GM12891	blood:	n/a
26	chr21:46494133-46494183	PrEC	prostate:	n/a
27	chr21:46494133-46494183	U87	brain:	n/a
28	chr21:46494133-46494183	NB4	blood:	n/a
29	chr21:46494133-46494183	HCF	heart:	n/a
30	chr21:46494133-46494183	HPAEpiC	pulmonary alveolar:	n/a
31	chr21:46494133-46494183	PFSK-1	brain:	n/a
32	chr21:46494133-46494183	K562	blood:	n/a
33	chr21:46494133-46494183	SAEC	small airway:	n/a
34	chr21:46494133-46494183	NT2-D1	testis:	n/a
35	chr21:46494133-46494183	SK-N-SH_RA	brain:	n/a
36	chr21:46494133-46494183	HAEpiC	amniotic membrane:	n/a
37	chr21:46494133-46494183	HL-60	blood:	n/a
38	chr21:46494133-46494183	BE2_C	brain:	n/a
39	chr21:46494133-46494183	HNPCEpiC	eye:	n/a
40	chr21:46494133-46494183	MCF10A-Er-Src	breast:	n/a
41	chr21:46494133-46494183	GM19239	blood:	n/a
42	chr21:46494133-46494183	HCT-116	colon:	n/a
43	chr21:46494133-46494183	Hepatocyte	liver:	n/a
44	chr21:46494133-46494183	RPTEC	kidney:	n/a
45	chr21:46494133-46494183	HMEC	breast:	n/a
46	chr21:46494133-46494183	SK-N-MC	brain:	n/a
47	chr21:46494133-46494183	HEEpiC	esophagus:	n/a
48	chr21:46494133-46494183	AG09309	skin:	n/a
49	chr21:46494133-46494183	A549	lung:	n/a
50	chr21:46494133-46494183	AG04450	lung:	fetal

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:31495841..31497461-chr21:46493757..46496010,2	K562	blood:
2	chr21:46354394..46357381-chr21:46492511..46494330,2	MCF-7	breast:
3	chr15:83679404..83681095-chr21:46492672..46494798,2	MCF-7	breast:
4	chr21:46231513..46241255-chr21:46492035..46497390,26	K562	blood:
5	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
6	chr21:46363747..46379047-chr21:46484156..46498795,67	K562	blood:
7	chr21:46492248..46501057-chr21:46545477..46562980,48	K562	blood:
8	chr21:46231904..46241990-chr21:46492035..46500735,28	K562	blood:
9	chr21:45526020..45528445-chr21:46493573..46495387,2	K562	blood:
10	chr21:46292697..46294233-chr21:46492293..46494359,2	K562	blood:
11	chr21:46358120..46360078-chr21:46493208..46495098,2	MCF-7	breast:
12	chr21:46355061..46362857-chr21:46490375..46496482,13	K562	blood:
13	chr21:46493165..46495720-chr21:46513762..46518212,6	MCF-7	breast:
14	chr21:46493210..46496355-chr21:46960101..46962644,7	K562	blood:
15	chr21:46493349..46495379-chr3:49062380..49065165,2	K562	blood:
16	chr21:45758282..45760774-chr21:46492663..46495375,2	K562	blood:
17	chr21:46493355..46495349-chr6:20402517..20405350,2	K562	blood:
18	chr21:46492507..46498258-chr21:46706665..46711571,8	K562	blood:
19	chr21:46220151..46222677-chr21:46492186..46495962,3	K562	blood:
20	chr21:46420509..46434696-chr21:46492036..46497081,20	K562	blood:
21	chr21:46382465..46395146-chr21:46491921..46496809,22	K562	blood:
22	chr21:46387463..46395588-chr21:46492597..46498092,12	K562	blood:
23	chr21:46492924..46497122-chr21:46547379..46551295,4	MCF-7	breast:
24	chr21:46345821..46352717-chr21:46492682..46495835,7	MCF-7	breast:
25	chr21:44393563..44395189-chr21:46493572..46495769,2	K562	blood:
26	chr21:46292272..46294074-chr21:46492667..46495373,2	MCF-7	breast:
27	chr21:46492557..46494672-chr5:76381901..76384633,2	MCF-7	breast:
28	chr21:46493305..46495041-chr21:46533530..46536007,3	K562	blood:
29	chr21:46329082..46330961-chr21:46492504..46494830,2	MCF-7	breast:
30	chr21:45553290..45555675-chr21:46493657..46496135,2	K562	blood:
31	chr21:46493602..46496021-chr6:27113430..27116414,2	K562	blood:
32	chr21:46493904..46495468-chr21:46952040..46954795,2	K562	blood:
33	chr19:40336793..40337645-chr21:46493997..46494626,2	HCT-116	colon:
34	chr21:46493837..46495534-chr21:46954524..46956701,2	K562	blood:
35	chr17:73775438..73776361-chr21:46493887..46494850,2	NB4	blood:
36	chr21:46422255..46425486-chr21:46493644..46496852,6	K562	blood:
37	chr21:46494154..46496164-chr21:46707875..46710753,3	K562	blood:
38	chr21:46330635..46333372-chr21:46493231..46495849,2	K562	blood:
39	chr21:46398654..46417262-chr21:46491498..46498908,48	K562	blood:
40	chr21:46348334..46352514-chr21:46492914..46497675,5	K562	blood:
41	chr21:46491911..46497737-chr21:46547142..46552694,13	K562	blood:
42	chr21:46413441..46419649-chr21:46493522..46496485,6	K562	blood:
43	chr21:46235651..46239241-chr21:46493223..46495632,4	MCF-7	breast:
44	chr21:46492324..46495855-chr21:46960806..46963103,3	K562	blood:
45	chr21:46493459..46495038-chr21:46842304..46845203,2	MCF-7	breast:
46	chr10:11207101..11207808-chr21:46493910..46494568,2	NB4	blood:
47	chr21:46493052..46496413-chr21:46547928..46550318,5	MCF-7	breast:
48	chr21:46493097..46497182-chr21:46538705..46543454,4	MCF-7	breast:
49	chr21:46493898..46494600-chr4:57301885..57302711,2	HCT-116	colon:
50	chr21:46411461..46416034-chr21:46491875..46495276,6	MCF-7	breast:

No data

Variant related genes	Relation type
SSR4P1	TF binding region
ENSG00000268856	TF binding region
ADARB1	TF binding region
SSR4P1	CpG island
ADARB1	CpG island
ENSG00000268856	CpG island
ENSG00000160256	Chromatin interaction
ENSG00000173638	Chromatin interaction
ENSG00000128050	Chromatin interaction
ENSG00000224930	Chromatin interaction
ENSG00000268805	Chromatin interaction
ENSG00000184787	Chromatin interaction
ENSG00000241945	Chromatin interaction
ENSG00000250802	Chromatin interaction
ENSG00000182871	Chromatin interaction
ENSG00000236519	Chromatin interaction
ENSG00000232969	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000169609	Chromatin interaction
ENSG00000183250	Chromatin interaction
ENSG00000105202	Chromatin interaction
ENSG00000186866	Chromatin interaction
ENSG00000197381	Chromatin interaction
ENSG00000272825	Chromatin interaction
ENSG00000273027	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000215447	Chromatin interaction
ENSG00000267857	Chromatin interaction
ENSG00000048740	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000184900	Chromatin interaction
ENSG00000160226	Chromatin interaction
ENSG00000183535	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000100478	Chromatin interaction
ENSG00000183255	Chromatin interaction
ENSG00000234880	Chromatin interaction
ENSG00000160199	Chromatin interaction
ENSG00000132846	Chromatin interaction
ENSG00000160221	Chromatin interaction
ENSG00000160255	Chromatin interaction
ENSG00000112242	Chromatin interaction
ENSG00000261706	Chromatin interaction
ENSG00000178035	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	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv834110	chr21:46316183-46505151	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
3	esv3355416	chr21:46492024-46497122	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
4	esv3409662	chr21:46492949-46495497	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	esv3342735	chr21:46493424-46495897	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	45 gene(s)	inside rSNPs	diseases
6	esv3325657	chr21:46493549-46496097	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46493200-46495000	Active TSS	Right Ventricle	heart
2	chr21:46493200-46495400	Active TSS	Fetal Brain Female	brain
3	chr21:46493200-46495400	Active TSS	NHLF	lung
4	chr21:46493200-46495800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr21:46493400-46494200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr21:46493400-46494800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr21:46493400-46494800	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr21:46493400-46494800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr21:46493400-46495000	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr21:46493400-46495000	Active TSS	Duodenum Mucosa	Duodenum
11	chr21:46493400-46495200	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr21:46493400-46495400	Active TSS	Rectal Smooth Muscle	rectum
13	chr21:46493400-46495400	Active TSS	A549	lung
14	chr21:46493400-46495600	Active TSS	Primary T cells from cord blood	blood
15	chr21:46493400-46495600	Active TSS	Primary T killer memory cells from peripheral blood	blood
16	chr21:46493400-46495800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr21:46493400-46495800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr21:46493400-46495800	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr21:46493400-46496000	Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr21:46493600-46494200	Active TSS	Fetal Kidney	kidney
21	chr21:46493600-46494200	Active TSS	Placenta	Placenta
22	chr21:46493600-46494400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr21:46493600-46494400	Active TSS	Fetal Muscle Trunk	muscle
24	chr21:46493600-46494800	Active TSS	H1 Cell Line	embryonic stem cell
25	chr21:46493600-46494800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr21:46493600-46494800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr21:46493600-46495000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr21:46493600-46495000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr21:46493600-46495000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr21:46493600-46495000	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr21:46493600-46495000	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr21:46493600-46495000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr21:46493600-46495000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr21:46493600-46495000	Active TSS	Fetal Stomach	stomach
35	chr21:46493600-46495000	Active TSS	Pancreas	Pancrea
36	chr21:46493600-46495000	Active TSS	Sigmoid Colon	Sigmoid Colon
37	chr21:46493600-46495000	Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr21:46493600-46495000	Active TSS	HepG2	liver
39	chr21:46493600-46495200	Active TSS	H9 Cell Line	embryonic stem cell
40	chr21:46493600-46495200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr21:46493600-46495200	Active TSS	Brain Germinal Matrix	brain
42	chr21:46493600-46495200	Active TSS	Fetal Muscle Leg	muscle
43	chr21:46493600-46495200	Active TSS	Gastric	stomach
44	chr21:46493600-46495200	Active TSS	Psoas Muscle	Psoas
45	chr21:46493600-46495200	Active TSS	K562	blood
46	chr21:46493600-46495400	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr21:46493600-46495400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr21:46493600-46495400	Active TSS	Brain Angular Gyrus	brain
49	chr21:46493600-46495400	Active TSS	Fetal Intestine Small	intestine
50	chr21:46493600-46495400	Active TSS	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links