Variant report

Variant	rs11247994
Chromosome Location	chr4:1343720-1343721
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:1343568-1343862	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1343700-1343750	AG09309	skin:	n/a
2	chr4:1343700-1343750	HCM	heart:	n/a
3	chr4:1343700-1343750	SAEC	small airway:	n/a
4	chr4:1343700-1343750	CMK	blood:	n/a
5	chr4:1343700-1343750	GM19239	blood:	n/a
6	chr4:1343700-1343750	NHBE	bronchial:	n/a
7	chr4:1343700-1343750	HEK293	kidney:	embryo
8	chr4:1343700-1343750	HRE	kidney:	n/a
9	chr4:1343700-1343750	BE2_C	brain:	n/a
10	chr4:1343700-1343750	Hepatocyte	liver:	n/a
11	chr4:1343700-1343750	NB4	blood:	n/a
12	chr4:1343700-1343750	U87	brain:	n/a
13	chr4:1343700-1343750	HRCEpiC	kidney:	n/a
14	chr4:1343700-1343750	GM12891	blood:	n/a
15	chr4:1343700-1343750	SK-N-SH_RA	brain:	n/a
16	chr4:1343700-1343750	ovcar-3	ovarian:	n/a
17	chr4:1343700-1343750	PANC-1	pancreas:	n/a
18	chr4:1343700-1343750	HCT-116	colon:	n/a
19	chr4:1343700-1343750	GM06990	blood:	n/a
20	chr4:1343700-1343750	MCF10A-Er-Src	breast:	n/a
21	chr4:1343700-1343750	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:1343700-1343750	HIPEpiC	eye:	n/a
23	chr4:1343700-1343750	HL-60	blood:	n/a
24	chr4:1343700-1343750	HEEpiC	esophagus:	n/a
25	chr4:1343700-1343750	PrEC	prostate:	n/a
26	chr4:1343700-1343750	A549	lung:	n/a
27	chr4:1343700-1343750	HUVEC	blood vessel:	n/a
28	chr4:1343700-1343750	BJ	skin:	n/a
29	chr4:1343700-1343750	NT2-D1	testis:	n/a
30	chr4:1343700-1343750	HCF	heart:	n/a
31	chr4:1343700-1343750	H1-hESC	embryonic stem cell:	embryo
32	chr4:1343700-1343750	Hela-S3	cervix:	n/a
33	chr4:1343700-1343750	HCPEpiC	choroid plexus:	n/a
34	chr4:1343700-1343750	AoSMC	blood vessel:	n/a
35	chr4:1343700-1343750	NH-A	brain:	n/a
36	chr4:1343700-1343750	Jurkat	blood:	n/a
37	chr4:1343700-1343750	RPTEC	kidney:	n/a
38	chr4:1343700-1343750	AG09319	gingival:	n/a
39	chr4:1343700-1343750	IMR90	lung:	fetal
40	chr4:1343700-1343750	GM12892	blood:	n/a
41	chr4:1343700-1343750	SK-N-SH	brain:	n/a
42	chr4:1343700-1343750	AG04450	lung:	fetal
43	chr4:1343700-1343750	MCF-7	breast:	n/a
44	chr4:1343700-1343750	AG10803	skin:	n/a
45	chr4:1343700-1343750	GM12878	blood:	n/a
46	chr4:1343700-1343750	T-47D	breast:	n/a
47	chr4:1343700-1343750	Caco-2	colon:	n/a
48	chr4:1343700-1343750	K562	blood:	n/a
49	chr4:1343700-1343750	PFSK-1	brain:	n/a
50	chr4:1343700-1343750	AG04449	skin:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1341512..1343900-chr4:1503503..1505335,2	K562	blood:
2	chr4:1338699..1344021-chr4:1351274..1357737,7	MCF-7	breast:
3	chr4:1236808..1249320-chr4:1336333..1343819,66	MCF-7	breast:
4	chr4:1282437..1287650-chr4:1338224..1344043,13	MCF-7	breast:
5	chr4:1343113..1345553-chr4:1365278..1367179,2	K562	blood:
6	chr4:1239325..1241522-chr4:1343447..1345640,2	K562	blood:
7	chr4:1287223..1288934-chr4:1342789..1345119,2	K562	blood:
8	chr4:1287434..1290416-chr4:1342936..1345119,2	K562	blood:
9	chr4:1235141..1249133-chr4:1336906..1347308,118	MCF-7	breast:
10	chr4:1280977..1287340-chr4:1335495..1344055,33	MCF-7	breast:
11	chr4:1239502..1245378-chr4:1336996..1344860,21	K562	blood:

No data

Variant related genes	Relation type
UVSSA	TF binding region
UVSSA	CpG island
ENSG00000253399	Chromatin interaction
ENSG00000159692	Chromatin interaction
ENSG00000090316	Chromatin interaction
ENSG00000196810	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs11247983	0.83[JPT][hapmap]
rs11247995	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11247996	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11247997	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11247998	0.81[CEU][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11721461	0.86[ASN][1000 genomes]
rs11724369	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11727167	0.83[JPT][hapmap]
rs11731853	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12502916	0.83[JPT][hapmap]
rs12512607	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.99[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12642410	0.82[JPT][hapmap]
rs13107446	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13112706	0.83[JPT][hapmap]
rs13113827	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13114537	0.91[CEU][hapmap];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13121833	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13128045	0.83[JPT][hapmap]
rs13128825	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13130329	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13134106	0.83[JPT][hapmap]
rs13134568	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13135102	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13135515	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13140040	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13140926	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13141169	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13141992	1.00[ASW][hapmap];0.85[CHB][hapmap];0.85[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13142985	0.96[CEU][hapmap];0.82[CHB][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.92[TSI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13145722	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13149575	0.83[JPT][hapmap]
rs13149952	0.83[JPT][hapmap]
rs13150571	0.90[JPT][hapmap]
rs1316393	0.82[ASW][hapmap];0.83[JPT][hapmap]
rs1732107	0.83[JPT][hapmap]
rs1960426	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs2141655	0.82[EUR][1000 genomes]
rs34299899	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35705197	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35735964	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35852462	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3796616	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3885694	0.89[GIH][hapmap];0.89[MEX][hapmap]
rs3915420	0.83[JPT][hapmap]
rs4246685	0.83[JPT][hapmap]
rs4405964	0.83[JPT][hapmap]
rs4428235	0.83[JPT][hapmap]
rs4516656	0.83[JPT][hapmap]
rs4519749	0.90[JPT][hapmap]
rs4642180	0.81[JPT][hapmap]
rs4974551	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4974552	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4974555	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4974582	0.89[JPT][hapmap]
rs4974602	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4974603	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4974604	1.00[CHB][hapmap]
rs4974605	1.00[CHB][hapmap]
rs4974607	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4974608	1.00[CHB][hapmap]
rs4974609	0.84[CEU][hapmap]
rs4974610	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4974619	0.96[CEU][hapmap];0.82[CHB][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6822570	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6826415	0.82[ASW][hapmap];0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7671242	0.96[CEU][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs900027	0.83[JPT][hapmap]
rs900028	0.83[JPT][hapmap]
rs900029	1.00[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats 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	121 gene(s)	inside rSNPs	diseases
5	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic 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 miRNA target site	71 gene(s)	inside rSNPs	diseases
6	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
8	nsv997971	chr4:1191256-1518521	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer 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 miRNA target site	67 gene(s)	inside rSNPs	diseases
9	nsv461155	chr4:1203265-1352685	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
10	nsv593281	chr4:1203265-1352685	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
11	nsv878338	chr4:1277826-1358449	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	nsv878339	chr4:1277826-1363886	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
13	nsv878340	chr4:1277826-1386570	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
14	nsv878341	chr4:1277826-1391400	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
15	nsv1002635	chr4:1282603-1402761	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
16	nsv878342	chr4:1291337-1363886	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
17	nsv878343	chr4:1291337-1391400	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
18	nsv878344	chr4:1291337-1414684	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
19	nsv878345	chr4:1291337-1563920	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	nsv461157	chr4:1300077-1352685	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
21	nsv593301	chr4:1300077-1352685	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
22	nsv878346	chr4:1300077-1363886	Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
23	nsv878347	chr4:1300077-1866358	Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
24	nsv878348	chr4:1305269-1386570	Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
25	esv1794294	chr4:1307119-1817474	Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
26	nsv878349	chr4:1318132-1363886	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
27	nsv878350	chr4:1320023-1500753	Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
28	nsv932661	chr4:1324751-1364014	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
29	nsv878351	chr4:1329847-1414684	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
30	nsv878352	chr4:1334721-1363886	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
31	nsv1008785	chr4:1335089-1518521	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
32	nsv536988	chr4:1335089-1518521	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
33	nsv593302	chr4:1338618-1414684	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs11247994	UVSSA	cis	Thyroid	GTEx
rs11247994	KIAA1530	cis	parietal	SCAN
rs11247994	MAEA	cis	Thyroid	GTEx
rs11247994	CTBP1	Cis_1M	lymphoblastoid	RTeQTL
rs11247994	CRIPAK	cis	Thyroid	GTEx
rs11247994	MAEA	cis	cerebellum	SCAN
rs11247994	CRIPAK	cis	cerebellum	SCAN
rs11247994	MAEA	cis	Nerve Tibial	GTEx
rs11247994	SCARNA22	cis	cerebellum	SCAN
rs11247994	CRIPAK	cis	parietal	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1341800-1346800	Weak transcription	Aorta	Aorta
2	chr4:1341800-1347000	Weak transcription	Ovary	ovary
3	chr4:1341800-1387800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:1341800-1388800	Weak transcription	Small Intestine	intestine
5	chr4:1342000-1343800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:1342000-1343800	Enhancers	Stomach Mucosa	stomach
7	chr4:1342000-1344200	Enhancers	Fetal Brain Male	brain
8	chr4:1342000-1344400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:1342000-1345800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:1342000-1351400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:1342200-1343800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr4:1342200-1345600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr4:1342200-1346200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr4:1342200-1354200	Weak transcription	NH-A	brain
15	chr4:1342200-1359400	Weak transcription	Right Atrium	heart
16	chr4:1342200-1369800	Weak transcription	HSMMtube	muscle
17	chr4:1342200-1382600	Weak transcription	Primary B cells from cord blood	blood
18	chr4:1342400-1343800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:1342400-1343800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:1342400-1344400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr4:1342400-1344600	Genic enhancers	Spleen	Spleen
22	chr4:1342400-1345400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:1342400-1345400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr4:1342400-1345600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr4:1342400-1346000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:1342400-1346000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:1342400-1346200	Weak transcription	Osteobl	bone
28	chr4:1342400-1346800	Weak transcription	Left Ventricle	heart
29	chr4:1342400-1350400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:1342400-1350600	Weak transcription	Fetal Lung	lung
31	chr4:1342400-1352600	Strong transcription	NHLF	lung
32	chr4:1342400-1370000	Weak transcription	HSMM	muscle
33	chr4:1342400-1379800	Weak transcription	A549	lung
34	chr4:1342600-1344600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:1342600-1345400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr4:1342600-1345400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr4:1342600-1345400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr4:1342600-1345400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr4:1342600-1345800	Weak transcription	Brain Anterior Caudate	brain
40	chr4:1342600-1346000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr4:1342600-1346200	Weak transcription	Liver	Liver
42	chr4:1342600-1349400	Weak transcription	K562	blood
43	chr4:1342600-1358400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:1342600-1367200	Weak transcription	Hela-S3	cervix
45	chr4:1342600-1385600	Weak transcription	Fetal Kidney	kidney
46	chr4:1342800-1344000	Weak transcription	Fetal Thymus	thymus
47	chr4:1342800-1344800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
48	chr4:1342800-1345600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr4:1342800-1346000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr4:1342800-1346200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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