Variant report

Variant	rs2267631
Chromosome Location	chr19:43100629-43100630
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	CTCF	chr19:43100613-43101112	HCT-116	colon:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
2	CTCF	chr19:43100566-43101077	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
3	SMC3	chr19:43100348-43101130	SK-N-SH	brain:	n/a	chr19:43100811-43100825
4	RAD21	chr19:43100618-43101007	SK-N-SH_RA	brain:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
5	CTCF	chr19:43100559-43101128	HCT-116	colon:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
6	CTCF	chr19:43100482-43101120	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
7	CTCF	chr19:43100623-43101013	Gliobla	brain:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
8	CTCF	chr19:43100545-43100990	H1-hESC	embryonic stem cell:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
9	CTCF	chr19:43099558-43101443	A549	lung:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100260-43100273 chr19:43100257-43100275 chr19:43100809-43100827 chr19:43100812-43100822
10	RAD21	chr19:43100574-43101054	MCF-7	breast:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
11	CTCF	chr19:43100486-43101071	A549	lung:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
12	RAD21	chr19:43100528-43101258	SK-N-SH	brain:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
13	CTCF	chr19:43100560-43101009	H1-hESC	embryonic stem cell:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
14	CTCF	chr19:43100491-43101198	GM12892	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
15	CTCF	chr19:43100587-43100988	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
16	CTCF	chr19:43100473-43101179	GM12891	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
17	MAX	chr19:43100622-43101129	K562	blood:	n/a	chr19:43100707-43100716
18	CTCF	chr19:43100610-43101074	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
19	CTCF	chr19:43100500-43101225	GM19239	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
20	RAD21	chr19:43100565-43101087	ECC-1	luminal epithelium:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
21	RAD21	chr19:43100621-43101073	MCF-7	breast:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
22	CTCF	chr19:43100600-43100890	A549	lung:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
23	CTCF	chr19:43100467-43101112	NHEK	skin:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
24	CTCF	chr19:43100622-43101000	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
25	CTCF	chr19:43100465-43100975	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
26	POLR2A	chr19:43100176-43100881	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:43100488-43101046	HepG2	liver:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
28	CTCF	chr19:43100592-43101094	GM12878	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
29	CTCF	chr19:43100516-43100639	GM13977	blood:	n/a	n/a
30	RAD21	chr19:43100567-43101048	HepG2	liver:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
31	CTCF	chr19:43100480-43101165	GM19240	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
32	RAD21	chr19:43100603-43101026	H1-hESC	embryonic stem cell:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
33	CTCF	chr19:43100622-43100949	GM13976	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
34	BHLHE40	chr19:43100628-43100974	K562	blood:	n/a	n/a
35	CTCF	chr19:43100626-43100995	GM12878	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
36	RAD21	chr19:43100576-43100993	HepG2	liver:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
37	RAD21	chr19:43100428-43101160	A549	lung:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
38	CTCF	chr19:43100560-43100710	HFF	foreskin:	n/a	chr19:43100656-43100669
39	CTCF	chr19:43100479-43100993	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
40	RAD21	chr19:43100477-43101171	HCT-116	colon:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
41	MYC	chr19:43100593-43100925	MCF-7	breast:	n/a	chr19:43100707-43100716
42	RAD21	chr19:43100622-43101003	HepG2	liver:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
43	RAD21	chr19:43100509-43101037	H1-hESC	embryonic stem cell:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
44	RAD21	chr19:43100531-43101069	A549	lung:	n/a	chr19:43100813-43100822 chr19:43100807-43100826
45	CTCF	chr19:43100428-43101010	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
46	CTCF	chr19:43100438-43101280	SK-N-SH	brain:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
47	ZNF143	chr19:43100583-43100986	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr19:43100628-43101019	IMR90	lung:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
49	MAX	chr19:43100609-43101111	MCF-7	breast:	n/a	chr19:43100707-43100716
50	RAD21	chr19:43100484-43101136	HCT-116	colon:	n/a	chr19:43100813-43100822 chr19:43100807-43100826

No.	Distal block	Cell Line	Cell type
1	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:
2	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:
3	chr19:42954441..42955205-chr19:43100309..43101289,2	MCF-7	breast:
4	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:

Variant related genes	Relation type
CEACAM8	TF binding region

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10401271	0.80[AMR][1000 genomes]
rs10402361	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10402401	0.87[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10402677	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10403517	0.88[CEU][hapmap];0.90[YRI][hapmap];0.82[AMR][1000 genomes]
rs10403979	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10404402	0.90[ASN][1000 genomes]
rs10404509	0.87[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10405445	0.82[AMR][1000 genomes]
rs10405646	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10405906	0.88[CEU][hapmap];0.93[YRI][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10407178	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10407576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10410147	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10411165	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10411458	0.96[ASN][1000 genomes]
rs10411945	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10412463	0.91[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10413014	0.87[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs10413413	0.88[CEU][hapmap];0.90[YRI][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10414602	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10415564	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10416089	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10417418	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10417693	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10419378	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10420164	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10420796	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10421108	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10421620	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10421881	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10422283	0.85[CHB][hapmap]
rs10422573	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10422987	0.85[ASN][1000 genomes]
rs10423291	0.96[ASN][1000 genomes]
rs10425241	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10469271	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10469285	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10469286	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1076243	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11083659	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11665767	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11665870	0.93[YRI][hapmap]
rs11666425	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11666835	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11666862	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11668009	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11668460	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11669892	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11670316	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11671846	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11673645	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11673684	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11879306	0.87[ASN][1000 genomes]
rs11881517	0.87[ASN][1000 genomes]
rs11882150	0.87[ASN][1000 genomes]
rs11882882	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12327586	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13346414	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975865	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs16975890	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1859341	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28411988	0.87[ASN][1000 genomes]
rs28447294	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2883270	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4499340	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55641435	0.96[ASN][1000 genomes]
rs55850134	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56237547	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56978333	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57902582	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59525393	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60052467	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs60313903	0.87[ASN][1000 genomes]
rs60662795	0.94[ASN][1000 genomes]
rs6509016	0.80[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6509017	0.96[ASN][1000 genomes]
rs6509020	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7247618	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7248042	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7248297	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7249411	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7253056	0.82[AMR][1000 genomes]
rs7253209	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73562329	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8102439	0.88[CEU][hapmap];0.83[YRI][hapmap]
rs8102519	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8103285	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8103891	0.87[ASN][1000 genomes]
rs8106083	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8106570	0.87[ASN][1000 genomes]
rs8107152	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8107254	0.90[YRI][hapmap]
rs8108816	0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8108844	0.87[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs8110766	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8110917	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8112156	0.82[AMR][1000 genomes]
rs851298	0.87[ASN][1000 genomes]
rs851301	0.87[ASN][1000 genomes]
rs851302	0.87[ASN][1000 genomes]
rs9304604	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
2	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	esv2422468	chr19:42991289-43669027	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1057390	chr19:43003323-43173028	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv482597	chr19:43037214-43222644	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2758501	chr19:43042747-43899053	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	esv2758763	chr19:43042747-43899053	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
8	nsv428023	chr19:43042747-43899053	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	esv2422227	chr19:43059426-43669485	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv3360773	chr19:43065661-43137022	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv1064734	chr19:43076046-43182478	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1058936	chr19:43082848-43228161	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	esv3331281	chr19:43087545-43124628	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv963055	chr19:43096862-43101157	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43099600-43100800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
2	chr19:43100200-43100800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:43100200-43100800	Enhancers	Primary B cells from cord blood	blood
4	chr19:43100400-43100800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:43100400-43101000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
6	chr19:43100400-43101000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
7	chr19:43100400-43101200	Enhancers	Adipose Nuclei	Adipose
8	chr19:43100600-43100800	Bivalent Enhancer	Placenta	Placenta
9	chr19:43100600-43101000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr19:43100600-43101000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr19:43100600-43101000	Enhancers	Right Ventricle	heart
12	chr19:43100600-43101000	Enhancers	Spleen	Spleen
13	chr19:43100600-43101200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
14	chr19:43100600-43101200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:43100600-43101200	Enhancers	Brain Cingulate Gyrus	brain
16	chr19:43100600-43101200	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr19:43100600-43101200	Bivalent Enhancer	HepG2	liver

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