Variant report

Variant	rs4880087
Chromosome Location	chr9:139963091-139963092
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:139962817..139966976-chr9:140133358..140138440,8	K562	blood:
2	chr9:139918787..139920491-chr9:139961520..139964011,2	MCF-7	breast:
3	chr9:139950787..139954133-chr9:139960532..139965214,5	MCF-7	breast:
4	chr9:139923344..139926131-chr9:139961105..139963789,2	K562	blood:
5	chr9:139942638..139950513-chr9:139960535..139967570,20	MCF-7	breast:
6	chr9:139962573..139965220-chr9:140094023..140096506,2	K562	blood:
7	chr9:139961438..139964036-chr9:140044543..140047199,2	K562	blood:
8	chr9:139961394..139967081-chr9:140115756..140120965,8	MCF-7	breast:
9	chr9:139960981..139963843-chr9:140097297..140100098,2	K562	blood:
10	chr9:139961125..139967160-chr9:140089646..140096252,9	MCF-7	breast:
11	chr9:139962510..139965497-chr9:139994905..139997427,2	MCF-7	breast:
12	chr9:139962339..139965028-chr9:140117731..140119279,2	K562	blood:
13	chr9:139959442..139968160-chr9:139974620..139981984,14	K562	blood:
14	chr9:139701776..139704316-chr9:139961341..139963993,2	MCF-7	breast:
15	chr9:139688767..139692141-chr9:139962525..139965411,3	MCF-7	breast:
16	chr9:139962921..139965561-chr9:139988478..139990333,2	K562	blood:
17	chr9:139961493..139963304-chr9:140137516..140140059,2	K562	blood:
18	chr9:139960749..139963302-chr9:140063195..140065389,2	K562	blood:
19	chr9:139942929..139945206-chr9:139962304..139965181,3	K562	blood:
20	chr9:139760746..139762936-chr9:139962388..139964127,2	MCF-7	breast:
21	chr9:139795452..139797956-chr9:139962617..139965206,2	MCF-7	breast:
22	chr9:139962929..139964657-chr9:140131246..140133354,2	MCF-7	breast:
23	chr9:139962243..139965148-chr9:140081432..140083970,3	MCF-7	breast:
24	chr9:139937349..139941097-chr9:139962279..139964529,3	K562	blood:
25	chr9:139842029..139844629-chr9:139961595..139963799,2	MCF-7	breast:
26	chr9:139961741..139964197-chr9:140006350..140009101,2	MCF-7	breast:
27	chr9:139938827..139942593-chr9:139960385..139966045,9	MCF-7	breast:
28	chr9:139951604..139953948-chr9:139961619..139963762,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000263697	Chromatin interaction
ENSG00000184925	Chromatin interaction
ENSG00000213213	Chromatin interaction
ENSG00000268996	Chromatin interaction
ENSG00000196642	Chromatin interaction
ENSG00000176248	Chromatin interaction
ENSG00000236394	Chromatin interaction
ENSG00000176101	Chromatin interaction
ENSG00000127191	Chromatin interaction
ENSG00000107281	Chromatin interaction
ENSG00000199411	Chromatin interaction
ENSG00000184709	Chromatin interaction
ENSG00000212864	Chromatin interaction
ENSG00000177239	Chromatin interaction
ENSG00000176978	Chromatin interaction
ENSG00000176058	Chromatin interaction
ENSG00000054179	Chromatin interaction
ENSG00000197191	Chromatin interaction
ENSG00000107331	Chromatin interaction
ENSG00000188229	Chromatin interaction
ENSG00000229257	Chromatin interaction
ENSG00000187713	Chromatin interaction
ENSG00000228544	Chromatin interaction

Extended variants
information (count: 127 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10117795	0.81[EUR][1000 genomes]
rs10747048	0.85[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs11145990	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11145996	0.85[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes]
rs1138628	0.84[ASW][hapmap];1.00[YRI][hapmap]
rs13631	0.90[JPT][hapmap]
rs17853460	0.86[MEX][hapmap]
rs2176675	0.84[ASW][hapmap]
rs3750517	0.86[ASW][hapmap];0.84[CEU][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs3750518	0.90[JPT][hapmap]
rs3763662	0.86[ASW][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs4880084	0.85[AFR][1000 genomes]
rs4880089	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];0.90[JPT][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4880091	0.84[ASW][hapmap];0.85[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs4880195	1.00[ASW][hapmap];0.89[CEU][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs4880197	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4880198	1.00[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4880199	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];0.90[JPT][hapmap];0.87[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4880200	0.85[CEU][hapmap];0.88[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs6420280	0.84[ASW][hapmap];0.85[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];0.87[MKK][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs6420281	0.81[EUR][1000 genomes]
rs6605	0.84[ASW][hapmap]
rs7037849	0.89[JPT][hapmap]
rs7467117	0.83[CHD][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs7853589	0.90[JPT][hapmap]
rs7856589	0.80[CHB][hapmap];0.95[JPT][hapmap]
rs7857270	0.85[JPT][hapmap]
rs9411242	1.00[ASW][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs9411245	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9411246	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9411299	0.84[ASW][hapmap];0.82[MEX][hapmap];1.00[YRI][hapmap]
rs9411304	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9411307	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs9411308	0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv540342	chr9:139218422-139973312	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	317 gene(s)	inside rSNPs	diseases
2	nsv469918	chr9:139254317-140068342	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh 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	341 gene(s)	inside rSNPs	diseases
3	nsv540346	chr9:139360142-140164011	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	471 gene(s)	inside rSNPs	diseases
4	nsv1039149	chr9:139376829-139991102	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	303 gene(s)	inside rSNPs	diseases
5	esv1803979	chr9:139395473-139979276	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised 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 miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
6	esv1831778	chr9:139395473-139979276	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
7	esv1821575	chr9:139395473-140068342	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
8	esv2422220	chr9:139478587-140244550	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	454 gene(s)	inside rSNPs	diseases
9	nsv894442	chr9:139544437-140462099	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
10	nsv894451	chr9:139598108-139995065	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
11	nsv894452	chr9:139598108-140523429	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
12	nsv894455	chr9:139607966-140411547	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh 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 miRNA target site	417 gene(s)	inside rSNPs	diseases
13	nsv894462	chr9:139683224-140274164	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	353 gene(s)	inside rSNPs	diseases
14	nsv894463	chr9:139683224-140411547	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
15	nsv524322	chr9:139690144-140376668	Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	371 gene(s)	inside rSNPs	diseases
16	nsv894469	chr9:139693992-140118448	Bivalent Enhancer Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
17	nsv894470	chr9:139693992-140339091	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	358 gene(s)	inside rSNPs	diseases
18	nsv894474	chr9:139694521-140432318	Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
19	nsv540352	chr9:139695108-140351178	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	358 gene(s)	inside rSNPs	diseases
20	nsv894483	chr9:139709976-139963091	Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	119 gene(s)	inside rSNPs	diseases
21	nsv894484	chr9:139709976-140382705	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong 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 miRNA target site	360 gene(s)	inside rSNPs	diseases
22	nsv894485	chr9:139709976-140408904	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh 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 miRNA target site	363 gene(s)	inside rSNPs	diseases
23	nsv894486	chr9:139725120-140382705	Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	359 gene(s)	inside rSNPs	diseases
24	nsv894487	chr9:139725120-140449582	Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
25	esv1803771	chr9:139776400-140274255	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers 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	321 gene(s)	inside rSNPs	diseases
26	nsv894498	chr9:139810595-140339091	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	324 gene(s)	inside rSNPs	diseases
27	nsv894499	chr9:139810595-140734161	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
28	esv1823828	chr9:139820363-140023694	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	121 gene(s)	inside rSNPs	diseases
29	esv1822764	chr9:139822266-140202692	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	313 gene(s)	inside rSNPs	diseases
30	nsv894501	chr9:139823670-140400275	Genic enhancers Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active 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	338 gene(s)	inside rSNPs	diseases
31	nsv894502	chr9:139823670-140487108	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
32	nsv894503	chr9:139830940-139987350	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
33	esv1834381	chr9:139834195-140031290	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	125 gene(s)	inside rSNPs	diseases
34	esv1823555	chr9:139834714-140362439	Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
35	nsv894506	chr9:139841512-140143801	Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	278 gene(s)	inside rSNPs	diseases
36	nsv894507	chr9:139860264-139995065	Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
37	nsv894515	chr9:139860631-139963091	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases
38	nsv894517	chr9:139860631-139977351	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	diseases
39	nsv894516	chr9:139860631-139979276	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
40	nsv894518	chr9:139860631-139995065	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
41	nsv466690	chr9:139860631-140042320	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	117 gene(s)	inside rSNPs	diseases
42	nsv615989	chr9:139860631-140042320	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	117 gene(s)	inside rSNPs	diseases
43	nsv615990	chr9:139860631-140068342	Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	118 gene(s)	inside rSNPs	diseases
44	nsv894519	chr9:139860631-140123584	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	161 gene(s)	inside rSNPs	diseases
45	nsv894520	chr9:139860631-140135118	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	185 gene(s)	inside rSNPs	diseases
46	nsv894521	chr9:139860631-140228092	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription 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	308 gene(s)	inside rSNPs	diseases
47	nsv894522	chr9:139860631-140411547	Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
48	nsv894523	chr9:139860631-140462099	Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
49	nsv1053902	chr9:139876167-139991102	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	103 gene(s)	inside rSNPs	diseases
50	nsv894547	chr9:139877698-139982868	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	103 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs4880087	EGFL7	cis	cerebellum	SCAN
rs4880087	UAP1L1	cis	Whole Blood	GTEx
rs4880087	C9orf142	cis	cerebellum	SCAN
rs4880087	TRAF2	cis	cerebellum	SCAN
rs4880087	ADAMTS13	cis	cerebellum	SCAN
rs4880087	LCN8	cis	cerebellum	SCAN
rs4880087	MAN1B1	cis	Whole Blood	GTEx
rs4880087	MAN1B1	cis	lung	GTEx
rs4880087	DPP7	Cis_1M	lymphoblastoid	RTeQTL
rs4880087	DPP7	cis	lymphoblastoid	seeQTL
rs4880087	LCNL1	cis	parietal	SCAN

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139949000-139963600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr9:139952200-139964000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:139952400-139963600	Weak transcription	HSMM	muscle
4	chr9:139955600-139963200	Weak transcription	NHLF	lung
5	chr9:139958600-139963600	Weak transcription	Fetal Brain Female	brain
6	chr9:139958600-139964000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:139958800-139963600	Weak transcription	Lung	lung
8	chr9:139959000-139963400	Weak transcription	Spleen	Spleen
9	chr9:139959000-139963600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr9:139959000-139963600	Weak transcription	Pancreas	Pancrea
11	chr9:139959000-139963800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:139959000-139963800	Weak transcription	Brain Anterior Caudate	brain
13	chr9:139959000-139963800	Weak transcription	Brain Substantia Nigra	brain
14	chr9:139959000-139964800	Weak transcription	Brain Angular Gyrus	brain
15	chr9:139959600-139964000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:139960000-139963400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr9:139960400-139963200	Weak transcription	Thymus	Thymus
18	chr9:139960400-139963800	Weak transcription	Gastric	stomach
19	chr9:139960800-139963200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:139961400-139963600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:139961800-139964400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr9:139962000-139963200	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr9:139962000-139963800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr9:139962000-139963800	Enhancers	Fetal Thymus	thymus
25	chr9:139962200-139963800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr9:139962400-139963200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr9:139962400-139963200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr9:139962400-139963200	Enhancers	Primary B cells from peripheral blood	blood
29	chr9:139962400-139963200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:139962400-139963200	Enhancers	Brain Germinal Matrix	brain
31	chr9:139962400-139963200	Enhancers	Duodenum Mucosa	Duodenum
32	chr9:139962400-139963200	Enhancers	Fetal Intestine Large	intestine
33	chr9:139962400-139963200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
34	chr9:139962400-139963200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr9:139962400-139963400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:139962400-139963400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr9:139962400-139963400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr9:139962400-139963400	Genic enhancers	Fetal Intestine Small	intestine
39	chr9:139962400-139963400	Flanking Active TSS	HepG2	liver
40	chr9:139962400-139963600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr9:139962400-139963600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr9:139962400-139963600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:139962400-139963600	Enhancers	A549	lung
44	chr9:139962400-139963600	Enhancers	HMEC	breast
45	chr9:139962400-139963800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:139962400-139963800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:139962400-139963800	Enhancers	Brain Hippocampus Middle	brain
48	chr9:139962400-139963800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr9:139962400-139963800	Enhancers	Right Ventricle	heart
50	chr9:139962400-139964000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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