Variant report

Variant	rs12662306
Chromosome Location	chr6:31511138-31511139
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr6:31510822-31511418	HepG2	liver:	n/a	n/a
2	POLR2A	chr6:31508618-31511594	HepG2	liver:	n/a	n/a
3	HEY1	chr6:31508765-31511176	K562	blood:	n/a	n/a
4	FOXA1	chr6:31511042-31511492	HepG2	liver:	n/a	n/a
5	FOXA1	chr6:31510738-31511412	HepG2	liver:	n/a	n/a
6	POLR2A	chr6:31505819-31511508	SK-N-MC	brain:	n/a	n/a
7	MXI1	chr6:31507514-31511487	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr6:31507792-31511234	PFSK-1	brain:	n/a	n/a

No data

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31508088..31512302-chr6:31792582..31797881,5	K562	blood:
2	chr6:31510898..31512528-chr6:31621703..31624538,2	MCF-7	breast:
3	chr6:31508752..31512657-chr6:31701865..31705930,6	K562	blood:
4	chr6:31509573..31511941-chr6:31658992..31661656,2	K562	blood:
5	chr6:31509627..31511469-chr6:31626737..31628735,4	MCF-7	breast:
6	chr6:31507082..31511713-chr6:31583957..31591905,17	MCF-7	breast:
7	chr6:31506561..31512642-chr6:31697539..31702106,5	K562	blood:
8	chr6:31510366..31512427-chr6:31782713..31784420,2	K562	blood:
9	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
10	chr6:31510807..31512542-chr6:31620152..31621684,2	MCF-7	breast:
11	chr6:31506496..31512275-chr6:31630248..31634828,11	K562	blood:
12	chr6:31508667..31511581-chr6:31742885..31745171,3	MCF-7	breast:
13	chr6:31510116..31512657-chr6:31703324..31705930,3	K562	blood:
14	chr6:31510463..31512638-chr6:31684771..31686477,2	MCF-7	breast:
15	chr6:31508080..31511338-chr6:31773122..31775825,3	K562	blood:
16	chr6:31506740..31512488-chr6:31586502..31592966,30	K562	blood:
17	chr6:31510094..31511838-chr6:31582401..31584650,2	K562	blood:
18	chr6:31509079..31511785-chr6:31559160..31560764,2	MCF-7	breast:
19	chr6:31510269..31511789-chr8:128582213..128583733,2	K562	blood:
20	chr6:31506595..31512441-chr6:31585525..31590767,30	K562	blood:
21	chr6:31508417..31511292-chr6:31625631..31629953,4	K562	blood:
22	chr6:31509573..31511196-chr6:31578119..31580506,2	K562	blood:
23	chr6:31510286..31512313-chr6:31556327..31558851,2	K562	blood:
24	chr6:31510287..31512759-chr6:31568800..31571526,2	K562	blood:
25	chr6:31509091..31511742-chr6:31868193..31871571,3	MCF-7	breast:
26	chr6:31507205..31511686-chr6:31618024..31622039,13	K562	blood:
27	chr6:31458384..31468965-chr6:31503613..31512721,28	K562	blood:
28	chr6:31509610..31511925-chr6:31559593..31562422,2	K562	blood:
29	chr6:31507998..31511841-chr6:31541735..31545245,5	MCF-7	breast:
30	chr6:31508169..31513281-chr6:31547465..31550370,6	K562	blood:
31	chr6:31507406..31516955-chr6:31615847..31623354,26	K562	blood:
32	chr6:31507927..31511187-chr6:31633283..31638231,4	MCF-7	breast:
33	chr6:31505350..31512312-chr6:31630543..31635379,11	K562	blood:
34	chr6:31507058..31511692-chr6:31586700..31590601,11	MCF-7	breast:
35	chr6:31509522..31512324-chr6:31604128..31605952,2	K562	blood:
36	chr6:31462628..31467072-chr6:31508179..31511597,8	MCF-7	breast:
37	chr6:31508700..31511164-chr6:32162690..32164850,2	K562	blood:
38	chr6:31460486..31468205-chr6:31503942..31512721,23	K562	blood:
39	chr6:31511090..31513028-chr6:31593636..31596148,2	K562	blood:
40	chr6:31507944..31511146-chr6:31743964..31746169,3	K562	blood:
41	chr6:31509889..31512472-chr6:31802635..31805585,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNORD84	TF binding region
NFKBIL1	TF binding region
DDX39B	TF binding region
ENSG00000204469	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000232810	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204475	Chromatin interaction
ENSG00000204301	Chromatin interaction
ENSG00000201680	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204472	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000204420	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000230622	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000240053	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000213719	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12665489	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12665501	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563350	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
4	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
5	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS 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 miRNA target site	370 gene(s)	inside rSNPs	diseases
6	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
7	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
8	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
9	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
10	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
11	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
12	nsv1018463	chr6:31337336-31525275	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
13	nsv538189	chr6:31337336-31525275	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
14	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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 miRNA target site	250 gene(s)	inside rSNPs	diseases
15	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
16	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
17	nsv432877	chr6:31412961-31528690	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
18	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
19	nsv470809	chr6:31496915-31544189	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic 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	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31508000-31511600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:31508200-31511400	Active TSS	GM12878-XiMat	blood
3	chr6:31508400-31511200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:31508400-31511200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:31508400-31511600	Active TSS	Psoas Muscle	Psoas
6	chr6:31508600-31511200	Active TSS	Colonic Mucosa	Colon
7	chr6:31509000-31511200	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr6:31509000-31511200	Active TSS	A549	lung
9	chr6:31509000-31511600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:31509400-31511400	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr6:31510000-31511200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr6:31510200-31511200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr6:31510400-31511200	Flanking Active TSS	Rectal Smooth Muscle	rectum
14	chr6:31510600-31511200	Enhancers	Primary B cells from cord blood	blood
15	chr6:31510600-31511200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:31510600-31511200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr6:31510600-31511200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr6:31510600-31511200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr6:31510600-31511400	Enhancers	Fetal Brain Male	brain
20	chr6:31510600-31511400	Enhancers	Fetal Heart	heart
21	chr6:31510600-31513200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:31510600-31513200	Weak transcription	Ovary	ovary
23	chr6:31510600-31513600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr6:31510600-31514200	Weak transcription	Aorta	Aorta
25	chr6:31510600-31514600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:31510600-31514600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr6:31510600-31515800	Weak transcription	Gastric	stomach
28	chr6:31510800-31511200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:31510800-31511200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:31510800-31511200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr6:31510800-31511200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr6:31510800-31511200	Enhancers	Primary hematopoietic stem cells	blood
33	chr6:31510800-31511200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:31510800-31511200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:31510800-31511200	Enhancers	Liver	Liver
36	chr6:31510800-31511200	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr6:31510800-31511200	Enhancers	Pancreas	Pancrea
38	chr6:31510800-31511200	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
39	chr6:31510800-31511200	Flanking Active TSS	Stomach Mucosa	stomach
40	chr6:31510800-31511200	Flanking Active TSS	Hela-S3	cervix
41	chr6:31510800-31511400	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr6:31510800-31511400	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr6:31510800-31511400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr6:31510800-31511400	Transcr. at gene 5' and 3'	Dnd41	blood
45	chr6:31510800-31511600	Flanking Active TSS	HepG2	liver
46	chr6:31510800-31513200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:31510800-31513200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr6:31510800-31513600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr6:31510800-31513800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr6:31510800-31514400	Weak transcription	Right Atrium	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links