Variant report

Variant	rs16894893
Chromosome Location	chr4:10205595-10205596
allele	A/T
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	ZBTB7A	chr4:10205581-10205795	K562	blood:	n/a	n/a
2	EP300	chr4:10205474-10206001	K562	blood:	n/a	n/a
3	ZNF384	chr4:10205029-10205989	K562	blood:	n/a	chr4:10205885-10205893
4	MAZ	chr4:10205295-10205962	K562	blood:	n/a	n/a
5	GATA2	chr4:10205537-10205877	K562	blood:	n/a	n/a
6	POLR2A	chr4:10205529-10205861	K562	blood:	n/a	n/a
7	CEBPB	chr4:10205485-10205827	K562	blood:	n/a	n/a
8	GATA2	chr4:10205525-10205800	K562	blood:	n/a	n/a
9	TEAD4	chr4:10205449-10205887	K562	blood:	n/a	n/a
10	TBP	chr4:10205467-10205841	K562	blood:	n/a	n/a
11	IRF1	chr4:10205361-10206112	K562	blood:	n/a	chr4:10205836-10205845
12	HMGN3	chr4:10205561-10205907	K562	blood:	n/a	n/a
13	TBL1XR1	chr4:10205528-10206379	K562	blood:	n/a	n/a
14	UBTF	chr4:10205483-10205958	K562	blood:	n/a	n/a
15	TEAD4	chr4:10205266-10206360	K562	blood:	n/a	chr4:10206205-10206214
16	RCOR1	chr4:10205116-10206189	K562	blood:	n/a	n/a
17	JUN	chr4:10205487-10206269	K562	blood:	n/a	chr4:10205646-10205657 chr4:10206155-10206163 chr4:10206076-10206088 chr4:10206155-10206162 chr4:10205645-10205653
18	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
19	ZMIZ1	chr4:10205586-10205883	K562	blood:	n/a	n/a
20	MYC	chr4:10205311-10206210	K562	blood:	n/a	n/a
21	JUND	chr4:10205395-10206315	K562	blood:	n/a	chr4:10205646-10205657 chr4:10206155-10206163 chr4:10206076-10206088 chr4:10206155-10206162 chr4:10205645-10205653
22	CBX3	chr4:10205085-10205934	K562	blood:	n/a	n/a
23	UBTF	chr4:10205522-10206086	K562	blood:	n/a	n/a
24	HDAC2	chr4:10205503-10205802	K562	blood:	n/a	n/a
25	MYC	chr4:10205564-10205958	K562	blood:	n/a	n/a
26	CEBPB	chr4:10204959-10205937	K562	blood:	n/a	chr4:10205836-10205844 chr4:10205110-10205121
27	HCFC1	chr4:10205555-10205869	K562	blood:	n/a	n/a
28	RCOR1	chr4:10205125-10205863	K562	blood:	n/a	n/a
29	MAX	chr4:10205534-10205897	K562	blood:	n/a	n/a
30	TBL1XR1	chr4:10205564-10205873	K562	blood:	n/a	n/a
31	MAFK	chr4:10205452-10205809	K562	blood:	n/a	n/a
32	CCNT2	chr4:10205478-10205881	K562	blood:	n/a	n/a
33	MAX	chr4:10205581-10205824	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10118560..10120526-chr4:10203986..10206288,3	K562	blood:
2	chr4:10199615..10202739-chr4:10203951..10206560,3	K562	blood:
3	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
4	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:

Variant related genes	Relation type
ENSG00000248777	TF binding region
ENSG00000248777	Chromatin interaction
ENSG00000071127	Chromatin interaction

Extended variants
information (count: 250 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:180)

rs_ID	r²[population]
rs10000104	0.86[ASN][1000 genomes]
rs10010656	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs10015494	0.82[CEU][hapmap]
rs10015872	0.82[CEU][hapmap]
rs10017447	0.95[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs10023177	0.91[CHB][hapmap]
rs10024152	0.95[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs10025456	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs10025980	0.84[ASN][1000 genomes]
rs10026434	0.92[ASN][1000 genomes]
rs10028503	0.82[CEU][hapmap]
rs10028937	0.82[CEU][hapmap]
rs10029208	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs10030776	0.95[CHB][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs10030782	0.95[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs10031453	0.82[CEU][hapmap]
rs10031694	0.84[ASN][1000 genomes]
rs10033955	0.89[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs10516200	0.81[CHB][hapmap]
rs10939722	0.82[CEU][hapmap]
rs10939730	0.83[CEU][hapmap]
rs10939732	0.82[CEU][hapmap]
rs10939766	0.95[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs10939801	0.95[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs10939829	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs11721530	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs11722345	0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs11723976	0.85[ASN][1000 genomes]
rs11724092	0.86[ASN][1000 genomes]
rs11724641	0.83[CHB][hapmap]
rs11726987	0.87[ASN][1000 genomes]
rs11726996	0.92[ASN][1000 genomes]
rs11727366	0.91[CHB][hapmap]
rs11727398	0.87[ASN][1000 genomes]
rs11730940	0.80[ASN][1000 genomes]
rs11731597	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs11732380	0.90[ASN][1000 genomes]
rs11732828	0.82[CEU][hapmap]
rs11734554	0.92[ASN][1000 genomes]
rs11734623	0.92[ASN][1000 genomes]
rs11737347	0.95[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs11937220	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs11947517	0.91[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs1468692	0.81[CEU][hapmap]
rs16868326	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs16894579	0.95[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs16895216	0.92[CEU][hapmap];0.87[YRI][hapmap]
rs1860896	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs1860907	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1990469	0.92[ASN][1000 genomes]
rs1990470	0.92[ASN][1000 genomes]
rs2068466	0.83[ASN][1000 genomes]
rs2080075	0.92[ASN][1000 genomes]
rs2080077	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs2098232	0.92[ASN][1000 genomes]
rs2098234	0.82[CHB][hapmap]
rs2098236	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs2159864	0.95[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs2159865	0.90[ASN][1000 genomes]
rs2192088	0.92[ASN][1000 genomes]
rs2192101	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs2215691	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs2241465	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs2241475	0.81[CHB][hapmap]
rs2241480	0.81[CHB][hapmap]
rs2241486	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs231	0.95[CHB][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs28414564	0.84[ASN][1000 genomes]
rs28496435	0.87[ASN][1000 genomes]
rs28507715	0.80[ASN][1000 genomes]
rs28528791	0.84[ASN][1000 genomes]
rs2868414	0.91[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs2868416	0.95[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs2868420	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs4168	0.83[CEU][hapmap]
rs4273473	0.95[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs4401449	0.83[CEU][hapmap]
rs4461524	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs4484300	0.82[CEU][hapmap]
rs4522862	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4574408	0.82[CEU][hapmap]
rs4697713	0.82[CEU][hapmap]
rs4697715	0.96[CEU][hapmap]
rs4697718	0.86[CHB][hapmap]
rs4697719	0.86[CHB][hapmap]
rs4697721	0.83[CHB][hapmap]
rs4697724	0.84[ASN][1000 genomes]
rs4697726	0.88[ASN][1000 genomes]
rs4697727	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs4697728	0.95[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs4697729	0.95[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs4697730	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs4697731	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs4697732	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs4697744	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs4697750	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4697751	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4697930	0.85[CEU][hapmap]
rs4697931	0.82[CEU][hapmap]
rs4697934	0.82[CEU][hapmap]
rs4697941	0.95[CHB][hapmap]
rs4697952	0.86[CHB][hapmap]
rs4697954	0.83[CHB][hapmap]
rs4697956	0.95[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs4697958	0.95[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs4697960	0.91[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs4697961	0.87[ASN][1000 genomes]
rs4697962	0.87[ASN][1000 genomes]
rs4697963	0.87[ASN][1000 genomes]
rs4697964	0.95[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs4697965	0.95[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs4697966	0.91[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs4697967	0.90[ASN][1000 genomes]
rs4697968	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs4697969	0.92[ASN][1000 genomes]
rs4697971	0.95[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs4697972	0.92[ASN][1000 genomes]
rs4697973	0.93[ASN][1000 genomes]
rs4697974	0.93[ASN][1000 genomes]
rs4697977	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs4697986	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4698025	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs55775442	0.92[ASN][1000 genomes]
rs55878266	0.92[ASN][1000 genomes]
rs56170676	0.80[ASN][1000 genomes]
rs56391253	0.87[ASN][1000 genomes]
rs56968294	0.81[EUR][1000 genomes]
rs57985219	0.82[ASN][1000 genomes]
rs62285986	0.87[ASN][1000 genomes]
rs6449342	0.90[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs6449351	0.90[ASN][1000 genomes]
rs6449355	0.95[CHB][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs6449438	0.92[CEU][hapmap]
rs66769576	0.92[ASN][1000 genomes]
rs6810699	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs6812780	0.82[CHB][hapmap];0.86[ASN][1000 genomes]
rs6813385	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs6823778	0.82[ASN][1000 genomes]
rs6826383	0.90[ASN][1000 genomes]
rs6826450	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs6829883	0.89[ASN][1000 genomes]
rs6830786	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs6832085	0.89[ASN][1000 genomes]
rs6836606	0.92[ASN][1000 genomes]
rs6844061	0.87[ASN][1000 genomes]
rs6845818	0.96[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6849583	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs6850516	0.82[CEU][hapmap]
rs6851536	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs6853056	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs6855489	0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs6855657	0.84[CEU][hapmap]
rs6858209	0.95[CHB][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs723663	0.95[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs723664	0.84[ASN][1000 genomes]
rs727995	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs734122	0.81[CHB][hapmap]
rs759031	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs7657551	0.95[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs7670376	0.95[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs7675945	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7690319	0.93[ASN][1000 genomes]
rs7692559	0.92[CEU][hapmap]
rs874079	0.86[CHB][hapmap]
rs887725	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs887727	0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs887728	0.95[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs887731	0.95[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs887734	0.84[ASN][1000 genomes]
rs917823	0.95[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs917824	0.88[CHB][hapmap];0.92[ASN][1000 genomes]
rs917825	0.95[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs917827	0.95[CHB][hapmap];0.81[JPT][hapmap]
rs9283699	0.95[CHB][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs9291661	0.81[ASN][1000 genomes]
rs956311	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs956312	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs9990501	0.85[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs9990701	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs9997234	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
2	nsv1014216	chr4:9713612-10223836	Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
3	nsv878681	chr4:9802853-10397327	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
4	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
5	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
6	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
7	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
9	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
10	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
11	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS 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	58 gene(s)	inside rSNPs	diseases
13	nsv537026	chr4:9903566-10262258	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
14	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
15	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
16	esv2752052	chr4:9911872-10313111	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
17	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
18	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
19	nsv532706	chr4:9948018-10451450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
20	nsv1013022	chr4:9961220-10230042	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
21	nsv537028	chr4:9961220-10230042	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
22	nsv537029	chr4:9961220-10262258	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
23	nsv878691	chr4:9966477-10418078	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
24	nsv1013487	chr4:9972011-10320963	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
25	nsv1008067	chr4:10004664-10262258	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
26	nsv537030	chr4:10004664-10262258	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
27	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
28	nsv537031	chr4:10040713-10262258	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
29	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
30	nsv428438	chr4:10058226-10273779	Flanking Active TSS Genic enhancers Strong transcription Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
31	nsv537032	chr4:10069805-10262258	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
32	nsv537033	chr4:10069805-10297561	Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
33	nsv1003286	chr4:10082156-10230606	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
34	esv16807	chr4:10099819-10234566	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
35	nsv537034	chr4:10103058-10262258	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
36	nsv537035	chr4:10103058-10297561	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
37	esv2752053	chr4:10124819-10270300	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
38	nsv593695	chr4:10138470-10345548	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
39	nsv1010383	chr4:10169535-10244955	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
40	nsv432577	chr4:10174139-10285348	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
41	esv10510	chr4:10174154-10234566	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
42	nsv998973	chr4:10178168-10236142	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
43	nsv508274	chr4:10179291-10239403	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
44	nsv1000149	chr4:10183420-10231486	Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
45	esv1817634	chr4:10186760-10246264	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
46	esv1811222	chr4:10191040-10235231	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
47	nsv1011718	chr4:10193427-10209251	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
48	nsv997862	chr4:10193427-10209934	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
49	esv2763832	chr4:10193427-10239297	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
50	esv1812062	chr4:10194269-10235231	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10204000-10205600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:10204200-10205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:10204600-10207400	Enhancers	HSMMtube	muscle
4	chr4:10205000-10205600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:10205000-10207800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:10205400-10205800	Enhancers	HMEC	breast
7	chr4:10205400-10206200	Flanking Active TSS	K562	blood
8	chr4:10205400-10206600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:10205400-10206800	Enhancers	HSMM	muscle
10	chr4:10205400-10207200	Enhancers	NHDF-Ad	bronchial

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