Variant report

Variant	rs8014760
Chromosome Location	chr14:35587767-35587768
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35587750-35587800	AoSMC	blood vessel:	n/a
2	chr14:35587750-35587800	SK-N-MC	brain:	n/a
3	chr14:35587750-35587800	RPTEC	kidney:	n/a
4	chr14:35587750-35587800	GM12892	blood:	n/a
5	chr14:35587750-35587800	AG10803	skin:	n/a
6	chr14:35587750-35587800	HL-60	blood:	n/a
7	chr14:35587750-35587800	PFSK-1	brain:	n/a
8	chr14:35587750-35587800	ECC-1	luminal epithelium:	n/a
9	chr14:35587750-35587800	NHBE	bronchial:	n/a
10	chr14:35587750-35587800	LNCaP	prostate:	n/a
11	chr14:35587750-35587800	HCT-116	colon:	n/a
12	chr14:35587750-35587800	GM06990	blood:	n/a
13	chr14:35587750-35587800	NH-A	brain:	n/a
14	chr14:35587750-35587800	MCF-7	breast:	n/a
15	chr14:35587750-35587800	SK-N-SH	brain:	n/a
16	chr14:35587750-35587800	GM12891	blood:	n/a
17	chr14:35587750-35587800	K562	blood:	n/a
18	chr14:35587750-35587800	HUVEC	blood vessel:	n/a
19	chr14:35587750-35587800	NT2-D1	testis:	n/a
20	chr14:35587750-35587800	U87	brain:	n/a
21	chr14:35587750-35587800	AG09319	gingival:	n/a
22	chr14:35587750-35587800	PrEC	prostate:	n/a
23	chr14:35587750-35587800	HMEC	breast:	n/a
24	chr14:35587750-35587800	PANC-1	pancreas:	n/a
25	chr14:35587750-35587800	H1-hESC	embryonic stem cell:	embryo
26	chr14:35587750-35587800	HCM	heart:	n/a
27	chr14:35587750-35587800	T-47D	breast:	n/a
28	chr14:35587750-35587800	HAEpiC	amniotic membrane:	n/a
29	chr14:35587750-35587800	NB4	blood:	n/a
30	chr14:35587750-35587800	Jurkat	blood:	n/a
31	chr14:35587750-35587800	HEK293	kidney:	embryo
32	chr14:35587750-35587800	Hela-S3	cervix:	n/a
33	chr14:35587750-35587800	HepG2	liver:	n/a
34	chr14:35587750-35587800	HRPEpiC	eye:	n/a
35	chr14:35587750-35587800	BE2_C	brain:	n/a
36	chr14:35587750-35587800	SK-N-SH_RA	brain:	n/a
37	chr14:35587750-35587800	HCPEpiC	choroid plexus:	n/a
38	chr14:35587750-35587800	GM19239	blood:	n/a
39	chr14:35587750-35587800	HIPEpiC	eye:	n/a
40	chr14:35587750-35587800	Hepatocyte	liver:	n/a
41	chr14:35587750-35587800	GM12878	blood:	n/a
42	chr14:35587750-35587800	HRCEpiC	kidney:	n/a
43	chr14:35587750-35587800	SAEC	small airway:	n/a
44	chr14:35587750-35587800	IMR90	lung:	fetal
45	chr14:35587750-35587800	MCF10A-Er-Src	breast:	n/a
46	chr14:35587750-35587800	AG09309	skin:	n/a
47	chr14:35587750-35587800	CMK	blood:	n/a
48	chr14:35587750-35587800	HCF	heart:	n/a
49	chr14:35587750-35587800	A549	lung:	n/a
50	chr14:35587750-35587800	SKMC	muscle:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35515793..35518719-chr14:35585868..35588915,3	K562	blood:
2	chr14:35585231..35589339-chr14:35589469..35593386,5	K562	blood:
3	chr14:35343360..35345155-chr14:35586268..35588307,2	MCF-7	breast:
4	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
5	chr14:35583719..35588379-chr14:35588655..35591956,6	MCF-7	breast:
6	chr14:35583308..35588876-chr14:35589178..35593731,8	MCF-7	breast:

No data

Variant related genes	Relation type
KIAA0391	CpG island
ENSG00000258790	CpG island
ENSG00000258738	Chromatin interaction
ENSG00000092020	Chromatin interaction
ENSG00000258790	Chromatin interaction
ENSG00000198604	Chromatin interaction
ENSG00000151327	Chromatin interaction
ENSG00000100890	Chromatin interaction

Extended variants
information (count: 129 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10137019	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10142846	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10144857	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10146133	0.91[ASN][1000 genomes]
rs10146691	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10149823	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs1064248	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11156874	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11848309	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11850487	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12100841	0.91[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.84[YRI][hapmap];0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12100944	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17103013	0.91[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs17103033	0.81[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.92[ASN][1000 genomes]
rs17103044	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.82[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17103047	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17103147	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17103166	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17386684	0.91[ASN][1000 genomes]
rs17456067	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1807162	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs2005535	1.00[CHB][hapmap]
rs2008130	0.81[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];1.00[ASN][1000 genomes]
rs2143948	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2143949	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2277459	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2277461	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2415258	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2415284	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs2899832	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34509212	0.91[ASN][1000 genomes]
rs4494460	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs55791227	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55833640	0.82[ASN][1000 genomes]
rs55890055	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56142562	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56363117	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57166048	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs57338667	0.87[ASN][1000 genomes]
rs57411359	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs60940685	0.81[ASN][1000 genomes]
rs61060564	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61492899	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62625039	0.91[ASN][1000 genomes]
rs6571694	0.91[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6571695	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6571709	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7140462	1.00[ASN][1000 genomes]
rs7154292	0.81[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.84[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7154637	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs7155697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7156704	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7156770	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7160889	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7218	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs72664814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664816	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72664819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72664829	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72664840	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72664843	0.91[ASN][1000 genomes]
rs72664849	0.84[ASN][1000 genomes]
rs72664854	0.91[ASN][1000 genomes]
rs72664855	0.91[ASN][1000 genomes]
rs72680622	0.87[ASN][1000 genomes]
rs72680641	0.87[ASN][1000 genomes]
rs72680648	0.96[ASN][1000 genomes]
rs72680652	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680655	1.00[ASN][1000 genomes]
rs72680657	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680662	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680663	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7493705	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs8004236	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8005079	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8007337	0.91[ASN][1000 genomes]
rs8007346	0.91[ASN][1000 genomes]
rs8007575	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8008066	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8009666	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8011195	0.91[ASN][1000 genomes]
rs8011242	1.00[ASN][1000 genomes]
rs8011549	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];1.00[ASN][1000 genomes]
rs8012905	0.96[ASN][1000 genomes]
rs8016140	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs8016541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017547	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8018116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8019182	1.00[ASN][1000 genomes]
rs8019482	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8019523	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8019700	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8019709	0.91[ASN][1000 genomes]
rs8019741	0.84[LWK][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs876996	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs9646144	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9888560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9888561	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9888597	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1043470	chr14:35398522-35754029	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv542031	chr14:35398522-35754029	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS 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	65 gene(s)	inside rSNPs	diseases
4	nsv901609	chr14:35449467-35587767	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS 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	52 gene(s)	inside rSNPs	diseases
5	nsv901613	chr14:35470049-35587767	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Enhancers Flanking Active TSS 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	30 gene(s)	inside rSNPs	diseases
6	nsv564264	chr14:35482797-35732369	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers 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
7	nsv901615	chr14:35485748-35630175	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv870305	chr14:35488290-35852349	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
9	nsv1052800	chr14:35509858-35607117	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers 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	37 gene(s)	inside rSNPs	diseases
10	nsv1044515	chr14:35510785-35756317	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers 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 target site	42 gene(s)	inside rSNPs	diseases
11	nsv564265	chr14:35512335-35624831	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats 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	38 gene(s)	inside rSNPs	diseases
12	nsv1046992	chr14:35527239-35724227	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats 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	27 gene(s)	inside rSNPs	diseases
13	nsv1051274	chr14:35529529-35724227	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv1048823	chr14:35537281-35724892	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats 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	27 gene(s)	inside rSNPs	diseases
15	nsv542032	chr14:35537281-35724892	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Enhancers 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	27 gene(s)	inside rSNPs	diseases
16	nsv1040540	chr14:35537481-35724753	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases
17	nsv542033	chr14:35537481-35724753	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
18	nsv1042625	chr14:35546094-35680358	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats 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	22 gene(s)	inside rSNPs	diseases
19	nsv1050123	chr14:35546114-35724892	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers 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	27 gene(s)	inside rSNPs	diseases
20	nsv542034	chr14:35546114-35724892	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking 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 target site	27 gene(s)	inside rSNPs	diseases
21	nsv1050700	chr14:35548276-35639084	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS 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	21 gene(s)	inside rSNPs	diseases
22	nsv1043692	chr14:35548276-35720016	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
23	nsv1053604	chr14:35548276-35825805	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
24	nsv542035	chr14:35563220-35607117	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
25	nsv1047992	chr14:35563220-35639084	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
26	nsv1052392	chr14:35563220-35893309	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
27	nsv542036	chr14:35563220-35893309	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
28	nsv1053978	chr14:35571762-35639084	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers 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	21 gene(s)	inside rSNPs	diseases
29	nsv534182	chr14:35579022-35620232	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
2	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
3	chr14:35542000-35589600	Weak transcription	Fetal Brain Male	brain
4	chr14:35545600-35590000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:35553400-35589800	Weak transcription	Pancreas	Pancrea
6	chr14:35564200-35589400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:35564800-35589800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr14:35577600-35589800	Strong transcription	Fetal Stomach	stomach
9	chr14:35579600-35590200	Weak transcription	Stomach Mucosa	stomach
10	chr14:35579800-35590000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:35580000-35589600	Weak transcription	Hela-S3	cervix
12	chr14:35580800-35590600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr14:35581400-35589800	Weak transcription	Gastric	stomach
14	chr14:35581400-35589800	Weak transcription	HMEC	breast
15	chr14:35581400-35589800	Weak transcription	NHEK	skin
16	chr14:35581400-35590000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:35581400-35590000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr14:35581400-35590000	Weak transcription	Psoas Muscle	Psoas
19	chr14:35581400-35590400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr14:35581400-35590400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr14:35581600-35590400	Weak transcription	Aorta	Aorta
22	chr14:35581800-35590000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr14:35582000-35590200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr14:35582800-35590000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:35582800-35590000	Weak transcription	Fetal Lung	lung
26	chr14:35583000-35589800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:35583000-35589800	Weak transcription	Colon Smooth Muscle	Colon
28	chr14:35583000-35590000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr14:35583000-35590000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:35583000-35590000	Weak transcription	Right Atrium	heart
31	chr14:35583000-35590000	Weak transcription	Small Intestine	intestine
32	chr14:35583000-35590000	Weak transcription	NHLF	lung
33	chr14:35583000-35590200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr14:35583200-35588600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr14:35583200-35589800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:35583200-35589800	Weak transcription	Ovary	ovary
37	chr14:35583200-35590000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr14:35583200-35590000	Weak transcription	HSMMtube	muscle
39	chr14:35583400-35589200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:35583400-35589400	Weak transcription	HUVEC	blood vessel
41	chr14:35583400-35589800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr14:35583400-35589800	Weak transcription	K562	blood
43	chr14:35583400-35590000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr14:35583400-35590000	Weak transcription	Brain Anterior Caudate	brain
45	chr14:35583400-35590000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr14:35583400-35590000	Weak transcription	Right Ventricle	heart
47	chr14:35583600-35588200	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr14:35583600-35589800	Weak transcription	A549	lung
49	chr14:35583600-35589800	Weak transcription	Osteobl	bone
50	chr14:35583600-35590000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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