Variant report

Variant	rs3730328
Chromosome Location	chr14:105240042-105240043
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	chr14:105239782-105240264	A549	lung:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
2	CTCF	chr14:105239940-105240090	AG04450	lung:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
3	RAD21	chr14:105239836-105240155	H1-hESC	embryonic stem cell:	n/a	chr14:105240030-105240043 chr14:105240031-105240040 chr14:105240032-105240044 chr14:105240027-105240046 chr14:105240028-105240042 chr14:105240032-105240042
4	MAFF	chr14:105239957-105240162	HepG2	liver:	n/a	chr14:105240066-105240084
5	CTCF	chr14:105239920-105240070	HA-sp	spinal cord:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
6	CTCF	chr14:105239980-105240130	HMF	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
7	POLR2A	chr14:105234595-105242540	HL-60	blood:	n/a	n/a
8	CTCF	chr14:105239980-105240130	WERI-Rb-1	eye:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
9	CTCF	chr14:105239980-105240130	Caco-2	colon:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
10	ELF1	chr14:105239877-105241343	MCF-7	breast:	n/a	chr14:105239951-105239963
11	CTCF	chr14:105239960-105240110	WERI-Rb-1	eye:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
12	MAX	chr14:105239475-105242482	MCF-7	breast:	n/a	chr14:105242321-105242330 chr14:105239768-105239778
13	POLR2A	chr14:105238502-105242352	HepG2	liver:	n/a	n/a
14	CTCF	chr14:105239880-105240170	A549	lung:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
15	CTCF	chr14:105239900-105240050	GM12878	blood:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
16	SMC3	chr14:105240000-105240063	HepG2	liver:	n/a	chr14:105240028-105240042 chr14:105240028-105240035
17	CTCF	chr14:105240000-105240150	AG09309	skin:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
18	MAFK	chr14:105239939-105240178	HepG2	liver:	n/a	chr14:105240067-105240082
19	CTCF	chr14:105239980-105240130	NHDF-neo	bronchial:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
20	CTCF	chr14:105239960-105240110	SAEC	small airway:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
21	CTCF	chr14:105239920-105240070	HBMEC	blood vessel:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
22	POLR2A	chr14:105240037-105240928	K562	blood:	n/a	n/a
23	CTCF	chr14:105239940-105240170	HFF	foreskin:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
24	CTCF	chr14:105239920-105240070	HEK293	kidney:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
25	CTCF	chr14:105239980-105240130	RPTEC	kidney:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
26	CTCF	chr14:105239979-105240047	IMR90	lung:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
27	CTCF	chr14:105239960-105240110	HCPEpiC	choroid plexus:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
28	ESR1	chr14:105239933-105240233	ECC-1	luminal epithelium:	n/a	n/a
29	CTCF	chr14:105239989-105240088	MCF-7	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
30	CTCF	chr14:105239965-105240136	Hela-S3	cervix:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
31	CTCF	chr14:105239969-105240117	MCF-7	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
32	RAD21	chr14:105239933-105240154	HepG2	liver:	n/a	chr14:105240030-105240043 chr14:105240031-105240040 chr14:105240032-105240044 chr14:105240027-105240046 chr14:105240028-105240042 chr14:105240032-105240042
33	CTCF	chr14:105239980-105240130	HepG2	liver:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
34	CTCF	chr14:105239980-105240130	MCF-7	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
35	CTCF	chr14:105239930-105240157	HepG2	liver:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
36	CTCF	chr14:105239936-105240070	H1-hESC	embryonic stem cell:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
37	POLR2A	chr14:105233017-105242484	HepG2	liver:	n/a	n/a
38	CTCF	chr14:105239920-105240070	SAEC	small airway:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
39	CTCF	chr14:105239960-105240110	HCFaa	heart:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
40	POLR2A	chr14:105239969-105240126	K562	blood:	n/a	n/a
41	CTCF	chr14:105239920-105240070	NHEK	skin:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
42	CTCF	chr14:105239940-105240090	AG04449	skin:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
43	RAD21	chr14:105239835-105240135	HepG2	liver:	n/a	chr14:105240030-105240043 chr14:105240031-105240040 chr14:105240032-105240044 chr14:105240027-105240046 chr14:105240028-105240042 chr14:105240032-105240042
44	CTCF	chr14:105239998-105240096	HepG2	liver:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
45	CTCF	chr14:105239990-105240098	MCF-7	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
46	CTCF	chr14:105239955-105240112	Pancreas_OC	pancreas:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
47	CTCF	chr14:105240000-105240150	HepG2	liver:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
48	CTCF	chr14:105239848-105240094	H1-hESC	embryonic stem cell:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
49	CTCF	chr14:105239940-105240090	Hela-S3	cervix:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
50	SMC3	chr14:105239933-105240133	Hela-S3	cervix:	n/a	chr14:105240028-105240042 chr14:105240028-105240035

No.	Distal block	Cell Line	Cell type
1	chr14:105239791..105242217-chr14:105329726..105333005,4	MCF-7	breast:
2	chr14:105217283..105220523-chr14:105237983..105243269,6	MCF-7	breast:
3	chr14:105238572..105242731-chr14:105243797..105248047,10	MCF-7	breast:
4	chr14:105218074..105222224-chr14:105239346..105242379,3	MCF-7	breast:
5	chr14:105239243..105243388-chr14:105243994..105248690,7	MCF-7	breast:
6	chr14:105239842..105240752-chr14:105259046..105260243,3	MCF-7	breast:

Variant related genes	Relation type
AKT1	TF binding region
ENSG00000184990	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000099814	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs3730345	1.00[AMR][1000 genomes]
rs58419996	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59947866	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360617	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360625	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73360636	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73360648	1.00[AMR][1000 genomes]
rs73362584	1.00[AMR][1000 genomes]
rs73362590	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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 miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	esv2830002	chr14:105078251-105348552	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
5	nsv902379	chr14:105086475-105274093	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv902387	chr14:105092479-105274093	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
7	nsv902388	chr14:105092479-105311249	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
8	nsv902389	chr14:105092479-105366499	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
9	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh 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	165 gene(s)	inside rSNPs	diseases
10	nsv902392	chr14:105105769-105274093	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv902394	chr14:105116232-105274093	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
12	nsv902396	chr14:105119897-105274093	Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
13	nsv470678	chr14:105126354-105246686	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
14	nsv566052	chr14:105126354-105268228	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
15	nsv470677	chr14:105126354-105348552	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
16	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
17	nsv566053	chr14:105139894-105268228	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
18	nsv902397	chr14:105139894-105268228	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
19	nsv517038	chr14:105146579-105311249	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
20	nsv566057	chr14:105146579-105311249	Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
21	nsv820230	chr14:105148655-105246686	ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
22	nsv566059	chr14:105148655-105268228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
23	nsv566060	chr14:105148655-105311249	Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS 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 target site	66 gene(s)	inside rSNPs	diseases
24	nsv902404	chr14:105148655-105311249	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
25	nsv902405	chr14:105148655-105340643	Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
26	nsv542226	chr14:105153660-105265857	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
27	nsv456455	chr14:105154105-105259734	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
28	nsv566062	chr14:105154105-105259734	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
29	nsv902407	chr14:105154105-105268228	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
30	nsv902408	chr14:105154105-105274093	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
31	nsv902409	chr14:105154105-105311249	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
32	nsv566063	chr14:105154105-105312935	Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS 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 target site	63 gene(s)	inside rSNPs	diseases
33	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
34	nsv902411	chr14:105163532-105268228	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
35	nsv566069	chr14:105185666-105274538	Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
36	nsv566070	chr14:105236355-105251720	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
37	nsv902412	chr14:105238701-105361934	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105221600-105253800	Weak transcription	Psoas Muscle	Psoas
2	chr14:105221800-105248200	Weak transcription	Fetal Brain Male	brain
3	chr14:105226200-105241600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr14:105235400-105251400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr14:105235400-105252600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr14:105235400-105259200	Strong transcription	NHLF	lung
7	chr14:105235400-105259400	Weak transcription	Right Atrium	heart
8	chr14:105235600-105244000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:105235600-105244200	Strong transcription	Fetal Brain Female	brain
10	chr14:105235600-105252600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr14:105235600-105255600	Strong transcription	Dnd41	blood
12	chr14:105235600-105257600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr14:105235800-105244000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:105235800-105249400	Strong transcription	Right Ventricle	heart
15	chr14:105236000-105242200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr14:105236000-105243600	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr14:105236000-105249600	Strong transcription	Stomach Smooth Muscle	stomach
18	chr14:105236200-105240600	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr14:105236200-105242200	Strong transcription	Skeletal Muscle Female	skeletal muscle
20	chr14:105236200-105243800	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr14:105236200-105244800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr14:105236200-105248400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr14:105236200-105249400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr14:105236400-105240200	Strong transcription	Placenta Amnion	Placenta Amnion
25	chr14:105236400-105243600	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr14:105236400-105247600	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr14:105236600-105247800	Strong transcription	Duodenum Mucosa	Duodenum
28	chr14:105236800-105242000	Strong transcription	Duodenum Smooth Muscle	Duodenum
29	chr14:105236800-105243400	Strong transcription	Brain Cingulate Gyrus	brain
30	chr14:105236800-105244600	Strong transcription	Primary T cells from cord blood	blood
31	chr14:105237000-105240200	Strong transcription	Rectal Smooth Muscle	rectum
32	chr14:105237000-105241000	Strong transcription	Brain Anterior Caudate	brain
33	chr14:105237000-105243000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr14:105237000-105243200	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr14:105237000-105243400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr14:105237000-105249600	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr14:105237200-105240200	Strong transcription	Primary B cells from cord blood	blood
38	chr14:105237200-105242200	Strong transcription	Left Ventricle	heart
39	chr14:105237200-105243200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:105237200-105243200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:105237200-105243600	Strong transcription	Brain Hippocampus Middle	brain
42	chr14:105237600-105241000	Weak transcription	Fetal Kidney	kidney
43	chr14:105237600-105241800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr14:105237600-105242000	Strong transcription	Aorta	Aorta
45	chr14:105237600-105242200	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr14:105237800-105241600	Strong transcription	Primary B cells from peripheral blood	blood
47	chr14:105237800-105243600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr14:105237800-105243600	Weak transcription	HMEC	breast
49	chr14:105238000-105240800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr14:105238000-105242200	Strong transcription	H9 Cell Line	embryonic stem cell

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