Variant report

Variant	rs2498801
Chromosome Location	chr14:105235558-105235559
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	chr14:105235440-105235590	AG04450	lung:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
2	CTCF	chr14:105235368-105235667	H1-hESC	embryonic stem cell:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
3	MAX	chr14:105234652-105235716	HepG2	liver:	n/a	chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235333-105235346 chr14:105235334-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235334-105235344 chr14:105235333-105235346 chr14:105235333-105235346 chr14:105235335-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235336-105235345
4	ELF1	chr14:105234595-105235661	MCF-7	breast:	n/a	chr14:105235518-105235530
5	CTCF	chr14:105235489-105235641	MCF-7	breast:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
6	CTCF	chr14:105235540-105235690	HBMEC	blood vessel:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
7	CTCF	chr14:105235511-105235625	MCF-7	breast:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
8	ELF1	chr14:105234614-105235653	GM12878	blood:	n/a	chr14:105235518-105235530
9	MAZ	chr14:105234689-105236220	IMR90	lung:	n/a	chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235333-105235346 chr14:105235334-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235334-105235344 chr14:105235333-105235346 chr14:105235333-105235346 chr14:105235335-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235336-105235345
10	CTCF	chr14:105235480-105235630	AG04449	skin:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
11	POLR2A	chr14:105234807-105235608	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr14:105234853-105235575	HepG2	liver:	n/a	n/a
13	CTCF	chr14:105235460-105235610	HPAF	blood vessel:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
14	CTCF	chr14:105235480-105235630	HA-sp	spinal cord:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
15	POLR2A	chr14:105235122-105235722	HepG2	liver:	n/a	n/a
16	USF1	chr14:105235143-105235575	H1-hESC	embryonic stem cell:	n/a	chr14:105235309-105235325
17	MAX	chr14:105234806-105235668	H1-hESC	embryonic stem cell:	n/a	chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235333-105235346 chr14:105235334-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235334-105235344 chr14:105235333-105235346 chr14:105235333-105235346 chr14:105235335-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235336-105235345
18	CTCF	chr14:105235480-105235630	HCPEpiC	choroid plexus:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
19	CTCF	chr14:105235520-105235670	HCFaa	heart:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
20	MYC	chr14:105234962-105235616	H1-hESC	embryonic stem cell:	n/a	chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235333-105235346 chr14:105235334-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235334-105235344 chr14:105235333-105235346 chr14:105235333-105235346 chr14:105235335-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235336-105235345
21	CTCF	chr14:105235480-105235630	HPAF	blood vessel:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
22	ZNF143	chr14:105234854-105235693	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr14:105235485-105235671	H1-hESC	embryonic stem cell:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
24	POLR2A	chr14:105234739-105239742	K562	blood:	n/a	n/a
25	CTCF	chr14:105235500-105235650	AG04450	lung:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
26	RAD21	chr14:105234715-105235792	H1-hESC	embryonic stem cell:	n/a	chr14:105235572-105235586 chr14:105235451-105235464 chr14:105235022-105235031 chr14:105235020-105235034 chr14:105235026-105235036 chr14:105235026-105235038 chr14:105235021-105235040 chr14:105235024-105235037
27	POLR2A	chr14:105234725-105235848	PANC-1	pancreas:	n/a	n/a
28	POLR2A	chr14:105234595-105242540	HL-60	blood:	n/a	n/a
29	CTCF	chr14:105235500-105235650	HMEC	breast:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
30	POLR2A	chr14:105235187-105235690	U87	brain:	n/a	n/a
31	RAD21	chr14:105234637-105235802	SK-N-SH	brain:	n/a	chr14:105235572-105235586 chr14:105235451-105235464 chr14:105235022-105235031 chr14:105235020-105235034 chr14:105235026-105235036 chr14:105235026-105235038 chr14:105235021-105235040 chr14:105235024-105235037
32	POLR2A	chr14:105234826-105235627	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr14:105234891-105235665	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr14:105232603-105238500	HepG2	liver:	n/a	n/a
35	NR2F2	chr14:105235128-105236103	K562	blood:	n/a	n/a
36	YY1	chr14:105234823-105235652	HepG2	liver:	n/a	chr14:105235317-105235328
37	MAX	chr14:105234618-105235735	MCF-7	breast:	n/a	chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235333-105235346 chr14:105235334-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235334-105235344 chr14:105235333-105235346 chr14:105235333-105235346 chr14:105235335-105235344 chr14:105235335-105235345 chr14:105235334-105235345 chr14:105235335-105235344 chr14:105235336-105235345
38	CTCF	chr14:105235486-105235659	K562	blood:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
39	POLR2A	chr14:105235141-105235657	GM12892	blood:	n/a	n/a
40	POLR2A	chr14:105234599-105235874	U87	brain:	n/a	n/a
41	POLR2A	chr14:105235125-105235635	HepG2	liver:	n/a	n/a
42	CTCF	chr14:105235440-105235590	GM12864	blood:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
43	CTCF	chr14:105235536-105235586	GM12891	blood:	n/a	chr14:105235573-105235582 chr14:105235573-105235586
44	POLR2A	chr14:105234667-105235698	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:105235440-105235590	GM12873	blood:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
46	CTCF	chr14:105235540-105235690	AG09319	gingival:	n/a	chr14:105235573-105235582 chr14:105235573-105235586 chr14:105235570-105235588
47	RAD21	chr14:105234644-105235704	HCT-116	colon:	n/a	chr14:105235572-105235586 chr14:105235451-105235464 chr14:105235022-105235031 chr14:105235020-105235034 chr14:105235026-105235036 chr14:105235026-105235038 chr14:105235021-105235040 chr14:105235024-105235037
48	JUND	chr14:105234523-105236150	MCF-7	breast:	n/a	n/a
49	POLR2A	chr14:105234838-105235571	H1-hESC	embryonic stem cell:	n/a	n/a
50	GABPA	chr14:105235120-105235699	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105219457..105221671-chr14:105233976..105237421,3	K562	blood:
2	chr14:105234590..105235623-chr14:105292148..105293402,8	K562	blood:
3	chr14:105155143..105157313-chr14:105233532..105235741,2	MCF-7	breast:
4	chr14:105206877..105208659-chr14:105234732..105236587,2	MCF-7	breast:
5	chr14:105234538..105236569-chr14:105286438..105288492,2	K562	blood:
6	chr14:105234579..105236355-chr14:105286684..105287712,12	MCF-7	breast:
7	chr14:105219054..105221939-chr14:105234928..105236625,2	MCF-7	breast:
8	chr14:105234268..105237912-chr14:105260331..105262677,3	K562	blood:

Variant related genes	Relation type
ENSG00000258430	TF binding region
ENSG00000185100	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000258701	Chromatin interaction
ENSG00000184990	Chromatin interaction
ENSG00000203485	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1132975	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12587551	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12590163	0.84[ASN][1000 genomes]
rs12889167	0.83[ASN][1000 genomes]
rs2494730	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2494731	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2494732	0.89[AFR][1000 genomes]
rs2494733	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2494734	0.86[ASN][1000 genomes]
rs2494735	0.85[ASN][1000 genomes]
rs2498796	0.89[ASN][1000 genomes]
rs2498797	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2498802	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2498803	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2498804	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28368454	0.92[EUR][1000 genomes]
rs3001371	0.88[ASN][1000 genomes]
rs3809453	0.84[ASN][1000 genomes]
rs45607139	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4983384	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4983544	0.82[ASN][1000 genomes]
rs4983546	0.82[ASN][1000 genomes]
rs4983549	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4983550	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57098433	0.83[EUR][1000 genomes]
rs60798007	0.83[EUR][1000 genomes]
rs60876857	0.82[EUR][1000 genomes]
rs66464514	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7151424	0.84[ASN][1000 genomes]
rs7158655	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7160733	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73362602	0.88[ASN][1000 genomes]
rs8006580	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8011461	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 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

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105221200-105236000	Weak transcription	Fetal Heart	heart
2	chr14:105221600-105253800	Weak transcription	Psoas Muscle	Psoas
3	chr14:105221800-105248200	Weak transcription	Fetal Brain Male	brain
4	chr14:105222800-105237400	Weak transcription	Fetal Kidney	kidney
5	chr14:105224200-105237200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr14:105224400-105237200	Weak transcription	Brain Substantia Nigra	brain
7	chr14:105225800-105238800	Weak transcription	Small Intestine	intestine
8	chr14:105226000-105237200	Weak transcription	Brain Angular Gyrus	brain
9	chr14:105226000-105237200	Weak transcription	NHDF-Ad	bronchial
10	chr14:105226000-105237600	Weak transcription	Aorta	Aorta
11	chr14:105226200-105241600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr14:105226400-105237000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:105226400-105237000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr14:105226600-105237000	Weak transcription	Colon Smooth Muscle	Colon
15	chr14:105226600-105237000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr14:105226600-105237200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr14:105227200-105236200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr14:105227200-105237200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr14:105227400-105237200	Weak transcription	Left Ventricle	heart
20	chr14:105228000-105236000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:105228000-105236200	Weak transcription	Gastric	stomach
22	chr14:105228000-105237200	Weak transcription	NHEK	skin
23	chr14:105228000-105237600	Weak transcription	GM12878-XiMat	blood
24	chr14:105228200-105237600	Weak transcription	HSMMtube	muscle
25	chr14:105228400-105237200	Weak transcription	Brain Hippocampus Middle	brain
26	chr14:105229000-105235800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr14:105229000-105236200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr14:105229000-105236800	Weak transcription	Primary T cells from cord blood	blood
29	chr14:105233000-105237200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr14:105233200-105237200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:105233200-105237400	Weak transcription	HSMM	muscle
32	chr14:105233600-105235600	Genic enhancers	Fetal Thymus	thymus
33	chr14:105233600-105236600	Genic enhancers	Spleen	Spleen
34	chr14:105233600-105236800	Genic enhancers	Fetal Muscle Trunk	muscle
35	chr14:105233600-105237600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:105233800-105235600	Enhancers	Lung	lung
37	chr14:105233800-105236800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:105234000-105235600	Enhancers	Liver	Liver
39	chr14:105234000-105236200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr14:105234400-105235800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:105234600-105235600	Enhancers	Primary T cells fromperipheralblood	blood
42	chr14:105234600-105235600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr14:105234600-105235600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr14:105234600-105235600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr14:105234600-105235600	Enhancers	Adipose Nuclei	Adipose
46	chr14:105234600-105235600	Enhancers	Colonic Mucosa	Colon
47	chr14:105234600-105235600	Genic enhancers	Fetal Intestine Small	intestine
48	chr14:105234600-105235600	Enhancers	Pancreas	Pancrea
49	chr14:105234600-105235600	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr14:105234600-105235600	Genic enhancers	Dnd41	blood

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