Variant report

Variant	rs7098372
Chromosome Location	chr10:5886149-5886150
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:30)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:30 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr10:5885832-5886170	GM12878	blood:	n/a	n/a
2	RUNX3	chr10:5885932-5886336	GM12878	blood:	n/a	n/a
3	RUNX3	chr10:5885619-5886502	GM12878	blood:	n/a	n/a
4	MEF2C	chr10:5885729-5886273	GM12878	blood:	n/a	n/a
5	EBF1	chr10:5885812-5886341	GM12878	blood:	n/a	chr10:5886190-5886201
6	POLR2A	chr10:5885729-5887374	GM12891	blood:	n/a	n/a
7	STAT5A	chr10:5886080-5886991	GM12878	blood:	n/a	chr10:5886768-5886776
8	ATF2	chr10:5885759-5886344	GM12878	blood:	n/a	n/a
9	PML	chr10:5885730-5887074	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:5885663-5886195	GM12878	blood:	n/a	n/a
11	PAX5	chr10:5885884-5886354	GM12891	blood:	n/a	n/a
12	MEF2A	chr10:5885754-5886254	GM12878	blood:	n/a	n/a
13	BCLAF1	chr10:5885619-5886233	GM12878	blood:	n/a	n/a
14	MEF2A	chr10:5885757-5886447	GM12878	blood:	n/a	chr10:5886257-5886278
15	TBP	chr10:5886050-5886186	GM12878	blood:	n/a	n/a
16	RCOR1	chr10:5885930-5886158	GM12878	blood:	n/a	n/a
17	RELA	chr10:5885788-5887156	GM12891	blood:	n/a	chr10:5886091-5886100 chr10:5886091-5886100
18	NFIC	chr10:5885610-5886992	GM12878	blood:	n/a	n/a
19	PAX5	chr10:5885971-5886312	GM12878	blood:	n/a	n/a
20	RELA	chr10:5885874-5887164	GM19099	blood:	n/a	chr10:5886091-5886100 chr10:5886091-5886100
21	BCL11A	chr10:5885938-5886268	GM12878	blood:	n/a	n/a
22	RELA	chr10:5885832-5886400	GM10847	blood:	n/a	chr10:5886091-5886100 chr10:5886091-5886100
23	NFATC1	chr10:5885623-5886208	GM12878	blood:	n/a	n/a
24	MTA3	chr10:5885741-5887324	GM12878	blood:	n/a	n/a
25	NRF1	chr10:5886149-5886263	GM12878	blood:	n/a	n/a
26	ZNF384	chr10:5885736-5886254	GM12878	blood:	n/a	n/a
27	NFIC	chr10:5885583-5886613	GM12878	blood:	n/a	n/a
28	FOXM1	chr10:5885640-5886456	GM12878	blood:	n/a	n/a
29	RELA	chr10:5885814-5887062	GM19193	blood:	n/a	chr10:5886091-5886100 chr10:5886091-5886100
30	ATF2	chr10:5885726-5886294	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5886111-5886161	ProgFib	skin:	n/a
2	chr10:5886111-5886161	HCT-116	colon:	n/a
3	chr10:5886111-5886161	HRE	kidney:	n/a
4	chr10:5886111-5886161	SK-N-SH	brain:	n/a
5	chr10:5886111-5886161	Hela-S3	cervix:	n/a
6	chr10:5886111-5886161	HRPEpiC	eye:	n/a
7	chr10:5886111-5886161	ovcar-3	ovarian:	n/a
8	chr10:5886111-5886161	A549	lung:	n/a
9	chr10:5886111-5886161	LNCaP	prostate:	n/a
10	chr10:5886111-5886161	PrEC	prostate:	n/a
11	chr10:5886111-5886161	K562	blood:	n/a
12	chr10:5886111-5886161	U87	brain:	n/a
13	chr10:5886111-5886161	GM12891	blood:	n/a
14	chr10:5886111-5886161	HCM	heart:	n/a
15	chr10:5886111-5886161	PANC-1	pancreas:	n/a
16	chr10:5886111-5886161	HUVEC	blood vessel:	n/a
17	chr10:5886111-5886161	HMEC	breast:	n/a
18	chr10:5886111-5886161	RPTEC	kidney:	n/a
19	chr10:5886111-5886161	HAEpiC	amniotic membrane:	n/a
20	chr10:5886111-5886161	GM12892	blood:	n/a
21	chr10:5886111-5886161	AG10803	skin:	n/a
22	chr10:5886111-5886161	NHBE	bronchial:	n/a
23	chr10:5886111-5886161	SK-N-MC	brain:	n/a
24	chr10:5886111-5886161	NB4	blood:	n/a
25	chr10:5886111-5886161	GM12878	blood:	n/a
26	chr10:5886111-5886161	PFSK-1	brain:	n/a
27	chr10:5886111-5886161	AG09319	gingival:	n/a
28	chr10:5886111-5886161	HNPCEpiC	eye:	n/a
29	chr10:5886111-5886161	H1-hESC	embryonic stem cell:	embryo
30	chr10:5886111-5886161	SKMC	muscle:	n/a
31	chr10:5886111-5886161	GM19239	blood:	n/a
32	chr10:5886111-5886161	GM06990	blood:	n/a
33	chr10:5886111-5886161	HepG2	liver:	n/a
34	chr10:5886111-5886161	AG04449	skin:	fetal
35	chr10:5886111-5886161	SK-N-SH_RA	brain:	n/a
36	chr10:5886111-5886161	HEEpiC	esophagus:	n/a
37	chr10:5886111-5886161	BE2_C	brain:	n/a
38	chr10:5886111-5886161	ECC-1	luminal epithelium:	n/a
39	chr10:5886111-5886161	HRCEpiC	kidney:	n/a
40	chr10:5886111-5886161	NH-A	brain:	n/a
41	chr10:5886111-5886161	AoSMC	blood vessel:	n/a
42	chr10:5886111-5886161	HCPEpiC	choroid plexus:	n/a
43	chr10:5886111-5886161	CMK	blood:	n/a
44	chr10:5886111-5886161	T-47D	breast:	n/a
45	chr10:5886111-5886161	Caco-2	colon:	n/a
46	chr10:5886111-5886161	Jurkat	blood:	n/a
47	chr10:5886111-5886161	IMR90	lung:	fetal
48	chr10:5886111-5886161	AG09309	skin:	n/a
49	chr10:5886111-5886161	HEK293	kidney:	embryo
50	chr10:5886111-5886161	HPAEpiC	pulmonary alveolar:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5854620..5857118-chr10:5886149..5888419,4	K562	blood:
2	chr10:5874603..5876795-chr10:5886014..5887751,3	MCF-7	breast:
3	chr10:5868411..5871104-chr10:5884225..5887747,3	K562	blood:
4	chr10:5852473..5857853-chr10:5880942..5888645,8	MCF-7	breast:
5	chr10:5851570..5858995-chr10:5881654..5887342,9	K562	blood:

No data

Variant related genes	Relation type
GDI2	TF binding region
GDI2	CpG island
ENSG00000057608	Chromatin interaction
ENSG00000272764	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10795590	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10795591	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10795593	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10795595	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10795596	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10905299	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10905302	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10905303	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10905307	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10905316	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11255549	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11255555	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11255558	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11255564	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11255577	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11255581	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11524382	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11819695	0.80[EUR][1000 genomes]
rs12246906	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12246907	0.89[AMR][1000 genomes]
rs12250878	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12253826	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12255077	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12359234	0.87[TSI][hapmap]
rs12774966	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12784539	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1512694	0.85[JPT][hapmap]
rs2104285	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2137423	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2203196	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2203197	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2380200	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2380201	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2380205	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2380208	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3954757	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4009521	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4256891	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4282894	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4282898	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4282899	0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4287254	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4293038	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4301704	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4330991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4421659	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4428973	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4468244	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4497300	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6602283	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6602284	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6602312	0.85[JPT][hapmap]
rs6602322	0.85[JPT][hapmap]
rs7072174	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7073128	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7099029	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs713588	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7894083	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7894559	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7897260	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7898042	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7898059	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7901964	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7902205	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7903875	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7904512	0.82[JPT][hapmap]
rs7906635	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7907053	0.85[JPT][hapmap]
rs7907795	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7907914	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7908028	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7919044	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7919785	0.85[JPT][hapmap]
rs7923278	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7923781	0.82[JPT][hapmap]
rs867052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs907685	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs907686	0.87[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs907688	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs907689	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9663697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9663995	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9732607	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv5654	chr10:5868365-5930634	Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv982902	chr10:5872818-5889953	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	esv3342274	chr10:5875995-5901345	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv1794948	chr10:5880066-5892545	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	esv1795821	chr10:5880066-5893268	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	esv1801910	chr10:5881740-5898882	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	esv1801679	chr10:5883033-5891501	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	esv1793088	chr10:5883308-5892545	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	esv3528067	chr10:5884196-5893994	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	esv3528068	chr10:5884196-5893994	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	esv1802022	chr10:5886149-5891501	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7098372	ANKRD16	cis	parietal	SCAN
rs7098372	ANKRD16	cis	cerebellum	SCAN

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5875000-5886600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:5882200-5886800	Weak transcription	NHLF	lung
3	chr10:5882600-5886800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:5882600-5888000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:5882800-5886800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:5882800-5886800	Weak transcription	NHDF-Ad	bronchial
7	chr10:5882800-5888200	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr10:5883000-5886200	Weak transcription	Placenta	Placenta
9	chr10:5883000-5886800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr10:5883000-5886800	Weak transcription	Left Ventricle	heart
11	chr10:5883000-5887000	Weak transcription	Adipose Nuclei	Adipose
12	chr10:5883200-5886400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr10:5883200-5887000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr10:5883200-5888000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:5883200-5897000	Enhancers	Primary B cells from peripheral blood	blood
16	chr10:5883400-5886800	Weak transcription	Brain Angular Gyrus	brain
17	chr10:5883400-5887000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr10:5883400-5887000	Weak transcription	Fetal Muscle Leg	muscle
19	chr10:5883400-5889000	Enhancers	Primary B cells from cord blood	blood
20	chr10:5883800-5888000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:5884000-5887400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr10:5885600-5886800	Enhancers	K562	blood
23	chr10:5885800-5886600	Enhancers	Fetal Heart	heart
24	chr10:5886000-5887200	Flanking Active TSS	GM12878-XiMat	blood
25	chr10:5886000-5888200	Enhancers	HepG2	liver

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