Variant report

Variant	rs7840687
Chromosome Location	chr8:86848522-86848523
allele	A/G
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	ATF3	chr8:86848176-86848532	K562	blood:	n/a	n/a
2	MYC	chr8:86848269-86848530	K562	blood:	n/a	chr8:86848385-86848394
3	FOSL2	chr8:86848086-86848577	SK-N-SH	brain:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
4	SMC3	chr8:86848166-86848582	Hela-S3	cervix:	n/a	n/a
5	JUN	chr8:86847631-86848762	K562	blood:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
6	SP1	chr8:86848099-86848606	A549	lung:	n/a	n/a
7	HDAC2	chr8:86848118-86848597	MCF-7	breast:	n/a	n/a
8	RFX5	chr8:86848142-86848645	Hela-S3	cervix:	n/a	n/a
9	FOXP2	chr8:86848176-86848561	SK-N-MC	brain:	n/a	n/a
10	SPI1	chr8:86848158-86848548	HL-60	blood:	n/a	n/a
11	EP300	chr8:86847775-86848569	Hela-S3	cervix:	n/a	chr8:86848385-86848394
12	STAT3	chr8:86848180-86848552	Hela-S3	cervix:	n/a	chr8:86848232-86848240 chr8:86848486-86848494
13	KAP1	chr8:86848132-86848540	U2OS	brain:	n/a	chr8:86848383-86848392
14	STAT3	chr8:86847605-86849659	MCF10A-Er-Src	breast:	n/a	chr8:86848232-86848240 chr8:86848486-86848494
15	FOSL1	chr8:86848177-86848606	K562	blood:	n/a	chr8:86848383-86848394 chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
16	ZNF143	chr8:86848229-86848564	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:86847793-86848810	A549	lung:	n/a	chr8:86848372-86848383
18	CEBPB	chr8:86848135-86848562	IMR90	lung:	n/a	chr8:86848372-86848383
19	MAX	chr8:86848426-86848628	K562	blood:	n/a	n/a
20	BACH1	chr8:86848360-86848557	K562	blood:	n/a	n/a
21	USF2	chr8:86848188-86848661	Hela-S3	cervix:	n/a	n/a
22	REST	chr8:86848084-86848524	PFSK-1	brain:	n/a	n/a
23	FOS	chr8:86847713-86848662	MCF10A-Er-Src	breast:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
24	SPI1	chr8:86848062-86848553	HL-60	blood:	n/a	n/a
25	SPI1	chr8:86848249-86848548	K562	blood:	n/a	n/a
26	TFAP2C	chr8:86848198-86849547	Hela-S3	cervix:	n/a	n/a
27	TAF1	chr8:86847834-86848560	PFSK-1	brain:	n/a	n/a
28	POLR2A	chr8:86848037-86849518	PFSK-1	brain:	n/a	n/a
29	TCF7L2	chr8:86848164-86849565	Hela-S3	cervix:	n/a	chr8:86848384-86848393
30	MAFK	chr8:86848199-86848564	K562	blood:	n/a	chr8:86848383-86848392
31	MYC	chr8:86847401-86848702	MCF10A-Er-Src	breast:	n/a	chr8:86848385-86848394
32	CEBPD	chr8:86848072-86848638	K562	blood:	n/a	chr8:86848307-86848318
33	REST	chr8:86848206-86848543	HL-60	blood:	n/a	n/a
34	CEBPB	chr8:86847869-86848819	K562	blood:	n/a	chr8:86848372-86848383
35	JUND	chr8:86848094-86848602	K562	blood:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848383-86848394 chr8:86848385-86848393 chr8:86848384-86848394
36	POLR2A	chr8:86848296-86848550	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr8:86847398-86849775	MCF10A-Er-Src	breast:	n/a	n/a
38	FOSL2	chr8:86848042-86848707	A549	lung:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
39	POLR2A	chr8:86848066-86849458	SK-N-MC	brain:	n/a	n/a
40	CEBPB	chr8:86848095-86848658	HCT-116	colon:	n/a	chr8:86848372-86848383
41	FOS	chr8:86847636-86848728	MCF10A-Er-Src	breast:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
42	CEBPD	chr8:86848089-86848561	K562	blood:	n/a	chr8:86848307-86848318
43	CBX3	chr8:86848116-86848555	K562	blood:	n/a	n/a
44	MAX	chr8:86848164-86848565	Hela-S3	cervix:	n/a	chr8:86848385-86848394
45	FOSL2	chr8:86848069-86848620	MCF-7	breast:	n/a	chr8:86848384-86848394 chr8:86848385-86848392 chr8:86848384-86848394 chr8:86848384-86848394 chr8:86848385-86848393 chr8:86848385-86848393 chr8:86848384-86848394
46	GTF2F1	chr8:86848127-86848546	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr8:86847614-86850294	PFSK-1	brain:	n/a	n/a
48	SPI1	chr8:86848254-86848532	K562	blood:	n/a	n/a
49	TAF1	chr8:86848173-86848524	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr8:86848087-86849637	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:86848347..86850172-chr8:86983643..86985301,2	MCF-7	breast:
2	chr8:86842328..86846143-chr8:86846375..86849662,4	K562	blood:
3	chr8:86843222..86846042-chr8:86847745..86849520,2	K562	blood:
4	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253154	TF binding region
ENSG00000104267	Chromatin interaction
ENSG00000253549	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11994093	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs1426569	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1484657	0.87[ASN][1000 genomes]
rs1484659	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs16898212	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16899237	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs16905281	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs17596760	0.88[CEU][hapmap]
rs1946380	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4378008	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4563937	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55994428	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56710369	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56894065	0.87[ASN][1000 genomes]
rs60186207	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62512062	0.87[ASN][1000 genomes]
rs62512065	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6471527	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6989561	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs7016015	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7016342	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs7016829	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7824910	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1804888	chr8:86263098-86986703	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv1807380	chr8:86405478-86886412	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv1829254	chr8:86405478-86886412	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv1831796	chr8:86405478-86886412	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	esv1807498	chr8:86405478-86986703	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	esv1828364	chr8:86405478-86986703	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	esv1831268	chr8:86405478-86986703	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
8	esv1844000	chr8:86405478-86986703	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	esv1851686	chr8:86405478-86986703	ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv427824	chr8:86405478-86986703	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	esv2758162	chr8:86405478-87055053	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	esv2759624	chr8:86405478-87055053	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv428204	chr8:86405478-87312208	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
14	nsv529563	chr8:86467090-87381984	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
15	nsv482395	chr8:86766289-86986303	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv6285	chr8:86775646-86866264	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	esv2764101	chr8:86785769-86918882	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
18	nsv33	chr8:86786398-86863566	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv469603	chr8:86790049-86956911	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
20	nsv482425	chr8:86790049-86956911	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
21	nsv891137	chr8:86827016-86899834	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
22	nsv891138	chr8:86827016-86914367	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
23	nsv891139	chr8:86827016-87001113	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
24	nsv1034791	chr8:86835367-86861743	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
25	nsv1016841	chr8:86835367-86865476	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv1023182	chr8:86835367-86879170	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
27	nsv1028959	chr8:86835367-87142383	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
28	nsv891140	chr8:86839183-86914367	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
29	nsv891141	chr8:86839183-86928990	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
30	nsv891142	chr8:86839183-86928990	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
31	nsv1018786	chr8:86840948-86921046	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
32	nsv1018255	chr8:86840948-86928885	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
33	nsv522895	chr8:86841229-86849334	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
34	nsv524454	chr8:86841229-86849334	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
35	nsv891144	chr8:86841229-86906419	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
36	nsv891143	chr8:86841229-86914367	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
37	nsv891145	chr8:86841229-86928990	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
38	nsv891146	chr8:86841229-87083747	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
39	nsv981883	chr8:86841289-86851534	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
40	nsv1034700	chr8:86843256-86900652	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
41	nsv1015386	chr8:86843256-86921046	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
42	nsv932023	chr8:86845979-87490694	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
43	nsv611672	chr8:86846445-86886950	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
44	nsv1032326	chr8:86848208-86871596	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86843000-86848600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:86843000-86848800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:86843600-86849000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:86844200-86849200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:86844600-86849000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:86845000-86848800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:86845800-86848600	Enhancers	Fetal Lung	lung
8	chr8:86845800-86849000	Weak transcription	HSMM	muscle
9	chr8:86845800-86849400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:86846200-86848600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr8:86846200-86848600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr8:86846200-86848600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:86846600-86849400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr8:86846800-86850400	Enhancers	Placenta Amnion	Placenta Amnion
15	chr8:86846800-86851600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr8:86847000-86848800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:86847000-86848800	Enhancers	NHEK	skin
18	chr8:86847000-86850400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:86847400-86848600	Enhancers	Muscle Satellite Cultured Cells	--
20	chr8:86847400-86851200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:86847800-86848600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr8:86847800-86848600	Enhancers	Liver	Liver
23	chr8:86847800-86848600	Enhancers	Placenta	Placenta
24	chr8:86847800-86848600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr8:86847800-86848800	Weak transcription	NHLF	lung
26	chr8:86848000-86848600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:86848000-86848600	Enhancers	Brain Substantia Nigra	brain
28	chr8:86848000-86849000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:86848200-86848600	Flanking Active TSS	K562	blood
30	chr8:86848200-86848800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr8:86848200-86848800	Enhancers	HMEC	breast
32	chr8:86848200-86848800	Weak transcription	HSMMtube	muscle
33	chr8:86848200-86849000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:86848200-86849000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:86848200-86849600	Active TSS	H9 Cell Line	embryonic stem cell
36	chr8:86848200-86854800	Weak transcription	Osteobl	bone
37	chr8:86848400-86848600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
38	chr8:86848400-86848800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:86848400-86848800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr8:86848400-86848800	Weak transcription	Adipose Nuclei	Adipose
41	chr8:86848400-86848800	Active TSS	Hela-S3	cervix
42	chr8:86848400-86848800	Weak transcription	NHDF-Ad	bronchial
43	chr8:86848400-86849000	Weak transcription	Brain Anterior Caudate	brain
44	chr8:86848400-86849000	Weak transcription	Brain Hippocampus Middle	brain
45	chr8:86848400-86849000	Active TSS	A549	lung
46	chr8:86848400-86849000	Weak transcription	NH-A	brain
47	chr8:86848400-86849200	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr8:86848400-86849400	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr8:86848400-86849400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:86848400-86849400	Active TSS	HUES48 Cell Line	embryonic stem cell

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