Variant report

Variant	rs17178952
Chromosome Location	chr6:29782126-29782127
allele	C/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	MAX	chr6:29782058-29782543	K562	blood:	n/a	n/a
2	TAL1	chr6:29782077-29783289	K562	blood:	n/a	n/a
3	JUND	chr6:29781582-29782530	K562	blood:	n/a	chr6:29781809-29781819 chr6:29781810-29781819 chr6:29781808-29781820 chr6:29781808-29781819 chr6:29781806-29781817 chr6:29781809-29781818
4	FOSL1	chr6:29781388-29782260	HCT-116	colon:	n/a	chr6:29781809-29781819 chr6:29781810-29781819 chr6:29781808-29781820 chr6:29781806-29781817 chr6:29781809-29781818
5	JUN	chr6:29781299-29782242	K562	blood:	n/a	chr6:29781809-29781819 chr6:29781810-29781819 chr6:29781808-29781820 chr6:29781806-29781817 chr6:29781809-29781818
6	FOSL1	chr6:29781352-29782146	HCT-116	colon:	n/a	chr6:29781809-29781819 chr6:29781810-29781819 chr6:29781808-29781820 chr6:29781806-29781817 chr6:29781809-29781818
7	ELF1	chr6:29781471-29782280	HCT-116	colon:	n/a	chr6:29781838-29781849 chr6:29781836-29781849
8	JUND	chr6:29781338-29782174	HCT-116	colon:	n/a	chr6:29781809-29781819 chr6:29781810-29781819 chr6:29781808-29781820 chr6:29781808-29781819 chr6:29781806-29781817 chr6:29781809-29781818
9	JUND	chr6:29781482-29782194	HCT-116	colon:	n/a	chr6:29781809-29781819 chr6:29781810-29781819 chr6:29781808-29781820 chr6:29781808-29781819 chr6:29781806-29781817 chr6:29781809-29781818

No.	Distal block	Cell Line	Cell type
1	chr6:29691597..29693774-chr6:29780569..29783300,2	MCF-7	breast:
2	chr6:29778199..29781037-chr6:29781139..29783059,2	K562	blood:
3	chr6:29776748..29779241-chr6:29782006..29784779,2	K562	blood:
4	chr6:29780662..29785245-chr6:29788028..29791562,7	K562	blood:
5	chr6:29712194..29714049-chr6:29781280..29783856,2	K562	blood:
6	chr6:29755654..29758226-chr6:29780556..29783054,2	MCF-7	breast:

Variant related genes	Relation type
MICG	TF binding region
ENSG00000225864	Chromatin interaction
ENSG00000237042	Chromatin interaction
ENSG00000204642	Chromatin interaction

Extended variants
information (count: 128 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs11751178	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11751201	0.83[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11751215	0.82[ASN][1000 genomes]
rs11751282	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11751333	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11751791	0.83[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11751820	0.83[AFR][1000 genomes]
rs11751848	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11752530	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11753654	0.94[AFR][1000 genomes]
rs11754253	0.83[AFR][1000 genomes]
rs11754577	1.00[AMR][1000 genomes]
rs11757126	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11757182	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11757480	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11757929	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11757937	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11757990	0.82[ASN][1000 genomes]
rs11758019	0.80[ASN][1000 genomes]
rs11758056	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11758087	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11759271	0.93[AMR][1000 genomes]
rs11759378	0.80[ASN][1000 genomes]
rs17178735	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17178749	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17178826	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17178938	0.81[EUR][1000 genomes]
rs17178989	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs17185244	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17185377	0.94[AFR][1000 genomes]
rs17185412	0.94[AFR][1000 genomes]
rs2272871	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2394176	0.94[AFR][1000 genomes]
rs2394177	0.94[AFR][1000 genomes]
rs2394696	0.91[AFR][1000 genomes]
rs2894117	1.00[AMR][1000 genomes]
rs34468824	0.94[AFR][1000 genomes]
rs34543080	0.88[AFR][1000 genomes]
rs34833819	0.83[AFR][1000 genomes]
rs35320382	0.91[AFR][1000 genomes]
rs35494442	0.89[AFR][1000 genomes]
rs3823321	0.91[AFR][1000 genomes]
rs3882583	0.89[AFR][1000 genomes]
rs3888720	0.94[AFR][1000 genomes]
rs3891162	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs3906248	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3998745	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4098859	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4409220	1.00[AMR][1000 genomes]
rs55868242	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56035102	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56221809	0.90[AFR][1000 genomes]
rs58449426	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58795395	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59416725	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59457386	0.94[AFR][1000 genomes]
rs59832006	0.89[AFR][1000 genomes]
rs59978815	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60299305	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60774155	0.94[AFR][1000 genomes]
rs61315420	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61331935	0.94[AFR][1000 genomes]
rs66472615	0.92[AFR][1000 genomes]
rs66776450	0.94[AFR][1000 genomes]
rs6915497	0.80[ASN][1000 genomes]
rs72492262	0.83[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs72492263	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72492266	0.85[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs72492268	0.82[ASN][1000 genomes]
rs72492271	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72492273	0.83[AFR][1000 genomes]
rs72492275	0.94[AFR][1000 genomes]
rs72492276	0.94[AFR][1000 genomes]
rs72492277	0.88[AFR][1000 genomes]
rs72492278	0.87[AFR][1000 genomes]
rs72492279	0.94[AFR][1000 genomes]
rs72492280	0.91[AFR][1000 genomes]
rs72492283	0.82[ASN][1000 genomes]
rs72507839	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72838212	0.92[AFR][1000 genomes]
rs72838213	0.94[AFR][1000 genomes]
rs72838218	0.91[AFR][1000 genomes]
rs72846618	0.94[AFR][1000 genomes]
rs72846685	0.94[AFR][1000 genomes]
rs72848310	0.94[AFR][1000 genomes]
rs73747518	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73747522	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73747524	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73747525	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73747534	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs73747573	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73747575	0.82[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs73747576	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7742733	0.92[AFR][1000 genomes]
rs7743372	0.94[AFR][1000 genomes]
rs7743930	0.94[AFR][1000 genomes]
rs7763677	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7769235	0.88[AFR][1000 genomes]
rs7769357	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv20940	chr6:29653954-29923410	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv428139	chr6:29659525-29892317	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
3	nsv427749	chr6:29659525-29975144	Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv10809	chr6:29692573-29794119	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv883532	chr6:29703262-29814963	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription 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	25 gene(s)	inside rSNPs	diseases
6	esv3441842	chr6:29715749-29942950	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	esv11180	chr6:29729381-29800066	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	esv3332677	chr6:29733187-29961463	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
9	esv3423001	chr6:29733216-29878601	Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
10	esv3475027	chr6:29733297-29922699	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	esv3475028	chr6:29733297-29922699	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	esv3420260	chr6:29734457-29835593	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
13	esv3330285	chr6:29736281-29881328	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
14	esv3396224	chr6:29754243-29888093	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
15	nsv965702	chr6:29758408-29798943	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
16	esv3430372	chr6:29759523-29974277	Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
17	esv3426050	chr6:29761594-29918407	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
18	esv3431350	chr6:29765473-29922767	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
19	nsv883540	chr6:29772395-29784317	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
20	esv3354193	chr6:29773857-29867902	Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
21	esv3451016	chr6:29774115-29929436	Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS 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 target site	32 gene(s)	inside rSNPs	diseases
22	esv3369144	chr6:29775824-29872385	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
23	esv3500392	chr6:29777854-29871802	Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
24	esv3500393	chr6:29777854-29871802	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
25	esv3352548	chr6:29777973-29783971	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
26	esv3384912	chr6:29778488-29872579	ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
27	esv3431922	chr6:29779132-29873171	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
28	esv3338581	chr6:29780045-29890754	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS 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	26 gene(s)	inside rSNPs	diseases
29	esv17468	chr6:29782014-29923275	Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29779400-29783800	Weak transcription	Right Atrium	heart
2	chr6:29780600-29782600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:29780600-29782800	Enhancers	HMEC	breast
4	chr6:29780800-29782800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:29781000-29783600	Enhancers	K562	blood
6	chr6:29781200-29782200	Enhancers	Hela-S3	cervix
7	chr6:29781600-29782200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:29781800-29782200	Enhancers	A549	lung
9	chr6:29781800-29782200	Bivalent Enhancer	HepG2	liver
10	chr6:29782000-29782400	Weak transcription	Placenta	Placenta
11	chr6:29782000-29783400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:29782000-29783600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:29782000-29783800	Weak transcription	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links