Variant report

Variant	esv1804053
Chromosome Location	chr14:24642785-24660721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1162)
CpG islands
(count:1221)
Chromatin interactive
region (count:62)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24657928-24658361	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24657961-24658316	K562	blood:	n/a	n/a
3	ATF1	chr14:24657976-24658310	K562	blood:	n/a	n/a
4	ATF2	chr14:24657707-24658471	GM12878	blood:	n/a	n/a
5	ATF2	chr14:24657751-24658453	GM12878	blood:	n/a	n/a
6	ATF2	chr14:24657918-24658369	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr14:24657918-24658402	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr14:24657807-24658404	A549	lung:	n/a	n/a
9	ATF3	chr14:24657757-24658366	A549	lung:	n/a	n/a
10	ATF3	chr14:24657882-24658365	K562	blood:	n/a	n/a
11	BATF	chr14:24657946-24658334	GM12878	blood:	n/a	n/a
12	BCL3	chr14:24657404-24658492	A549	lung:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
13	BCL3	chr14:24657689-24658339	GM12878	blood:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
14	BCL3	chr14:24657494-24658458	A549	lung:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
15	BCLAF1	chr14:24657872-24658327	K562	blood:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
16	BCLAF1	chr14:24657625-24658473	GM12878	blood:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
17	BCLAF1	chr14:24657917-24658283	K562	blood:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
18	BCLAF1	chr14:24650956-24651718	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:24657811-24658366	GM12878	blood:	n/a	chr14:24658152-24658161 chr14:24658066-24658075
20	BHLHE40	chr14:24657596-24658336	K562	blood:	n/a	n/a
21	BHLHE40	chr14:24657474-24658353	HepG2	liver:	n/a	n/a
22	BHLHE40	chr14:24657892-24658286	A549	lung:	n/a	n/a
23	BHLHE40	chr14:24657782-24658254	HepG2	liver:	n/a	n/a
24	BHLHE40	chr14:24657632-24658462	GM12878	blood:	n/a	n/a
25	BRCA1	chr14:24657980-24658319	GM12878	blood:	n/a	n/a
26	BRCA1	chr14:24657496-24657674	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr14:24657906-24658317	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr14:24657990-24658353	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr14:24657582-24658343	HepG2	liver:	n/a	n/a
30	CBX3	chr14:24658003-24658281	K562	blood:	n/a	n/a
31	CBX3	chr14:24657809-24658354	K562	blood:	n/a	n/a
32	CCNT2	chr14:24657496-24658260	K562	blood:	n/a	chr14:24658027-24658036 chr14:24657528-24657537
33	CEBPB	chr14:24657944-24658277	K562	blood:	n/a	n/a
34	CEBPB	chr14:24657736-24658382	MCF-7	breast:	n/a	n/a
35	CEBPB	chr14:24649328-24649520	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:24657882-24658230	K562	blood:	n/a	n/a
37	CEBPB	chr14:24657863-24658487	GM12878	blood:	n/a	n/a
38	CEBPB	chr14:24657872-24658329	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr14:24657879-24658331	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:24657879-24658331	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:24657470-24657602	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr14:24657940-24658323	A549	lung:	n/a	n/a
43	CEBPB	chr14:24657920-24658330	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:24657767-24658394	A549	lung:	n/a	n/a
45	CEBPB	chr14:24657925-24658393	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPD	chr14:24657918-24658317	K562	blood:	n/a	n/a
47	CEBPD	chr14:24657817-24658350	HepG2	liver:	n/a	n/a
48	CEBPD	chr14:24657376-24658344	HepG2	liver:	n/a	n/a
49	CEBPZ	chr14:24659164-24659276	HepG2	liver:	n/a	n/a
50	CHD1	chr14:24657596-24658325	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24653711-24653761	BE2_C	brain:	n/a
2	chr14:24653711-24653761	BE2_C	brain:	n/a
3	chr14:24658182-24658232	AG10803	skin:	n/a
4	chr14:24657962-24658012	SK-N-SH	brain:	n/a
5	chr14:24659193-24659243	AG09319	gingival:	n/a
6	chr14:24658249-24658299	Hepatocyte	liver:	n/a
7	chr14:24658731-24658781	ovcar-3	ovarian:	n/a
8	chr14:24657797-24657847	HAEpiC	amniotic membrane:	n/a
9	chr14:24649335-24649385	NT2-D1	testis:	n/a
10	chr14:24657526-24657576	CMK	blood:	n/a
11	chr14:24658256-24658306	AG10803	skin:	n/a
12	chr14:24658292-24658342	HCF	heart:	n/a
13	chr14:24644504-24644554	ovcar-3	ovarian:	n/a
14	chr14:24658292-24658342	GM19239	blood:	n/a
15	chr14:24658184-24658234	Caco-2	colon:	n/a
16	chr14:24658182-24658232	Hepatocyte	liver:	n/a
17	chr14:24657962-24658012	Hela-S3	cervix:	n/a
18	chr14:24659193-24659243	GM19239	blood:	n/a
19	chr14:24649335-24649385	RPTEC	kidney:	n/a
20	chr14:24658841-24658891	SK-N-MC	brain:	n/a
21	chr14:24658249-24658299	ovcar-3	ovarian:	n/a
22	chr14:24658841-24658891	Jurkat	blood:	n/a
23	chr14:24658101-24658151	HUVEC	blood vessel:	n/a
24	chr14:24658292-24658342	MCF-7	breast:	n/a
25	chr14:24658731-24658781	HCF	heart:	n/a
26	chr14:24659193-24659243	ECC-1	luminal epithelium:	n/a
27	chr14:24658182-24658232	NB4	blood:	n/a
28	chr14:24658124-24658174	PrEC	prostate:	n/a
29	chr14:24658101-24658151	K562	blood:	n/a
30	chr14:24657797-24657847	IMR90	lung:	fetal
31	chr14:24658249-24658299	HEK293	kidney:	embryo
32	chr14:24657797-24657847	AG04449	skin:	fetal
33	chr14:24657526-24657576	A549	lung:	n/a
34	chr14:24658124-24658174	A549	lung:	n/a
35	chr14:24659386-24659436	MCF-7	breast:	n/a
36	chr14:24658256-24658306	HIPEpiC	eye:	n/a
37	chr14:24657797-24657847	GM06990	blood:	n/a
38	chr14:24658143-24658193	HL-60	blood:	n/a
39	chr14:24658184-24658234	PANC-1	pancreas:	n/a
40	chr14:24658249-24658299	HUVEC	blood vessel:	n/a
41	chr14:24658292-24658342	HAEpiC	amniotic membrane:	n/a
42	chr14:24658101-24658151	AG04449	skin:	fetal
43	chr14:24658256-24658306	U87	brain:	n/a
44	chr14:24658099-24658149	GM12878	blood:	n/a
45	chr14:24658731-24658781	K562	blood:	n/a
46	chr14:24658292-24658342	A549	lung:	n/a
47	chr14:24658182-24658232	GM12892	blood:	n/a
48	chr14:24658292-24658342	HRE	kidney:	n/a
49	chr14:24658731-24658781	HEK293	kidney:	embryo
50	chr14:24657797-24657847	MCF10A-Er-Src	breast:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:24658469..24661265-chr14:24739057..24740636,2	K562	blood:
2	chr11:71158745..71161047-chr14:24656517..24659263,2	MCF-7	breast:
3	chr14:24640332..24642740-chr14:24644969..24648486,4	K562	blood:
4	chr14:23790288..23791874-chr14:24656681..24658502,2	MCF-7	breast:
5	chr14:24601126..24603533-chr14:24656330..24657992,2	K562	blood:
6	chr14:24641149..24643201-chr14:24656538..24659107,2	K562	blood:
7	chr14:24026023..24030231-chr14:24656476..24659389,3	MCF-7	breast:
8	chr14:24570842..24573550-chr14:24657440..24659369,2	MCF-7	breast:
9	chr14:24603743..24605973-chr14:24646777..24648838,2	K562	blood:
10	chr14:24629833..24630577-chr14:24657173..24657821,2	MCF-7	breast:
11	chr14:24653860..24661964-chr14:24680820..24687057,41	MCF-7	breast:
12	chr14:24654479..24657858-chr14:24783212..24786979,3	K562	blood:
13	chr14:24659710..24661971-chr14:24783467..24786421,2	K562	blood:
14	chr14:24562605..24564196-chr14:24654231..24655795,2	K562	blood:
15	chr14:24628862..24633065-chr14:24656261..24659048,5	K562	blood:
16	chr14:24656637..24660595-chr14:24683855..24686255,4	K562	blood:
17	chr14:24581352..24586794-chr14:24656349..24659951,9	MCF-7	breast:
18	chr14:24656442..24659058-chr14:24740338..24741851,2	MCF-7	breast:
19	chr14:24641149..24643201-chr14:24656538..24659107,2	K562	blood:
20	chr14:24655312..24660662-chr14:24700172..24703885,7	MCF-7	breast:
21	chr14:24655487..24659760-chr14:24674840..24680491,9	MCF-7	breast:
22	chr14:24657460..24658413-chr7:139026058..139026681,2	NB4	blood:
23	chr1:153506024..153506652-chr14:24657445..24658442,2	Hela-S3	cervix:
24	chr14:24629039..24631896-chr14:24646822..24648474,2	K562	blood:
25	chr14:24655787..24658216-chr14:24740858..24744211,3	K562	blood:
26	chr14:24563470..24565156-chr14:24656534..24660017,3	K562	blood:
27	chr14:24583410..24585426-chr14:24647277..24649187,2	MCF-7	breast:
28	chr14:24561763..24563268-chr14:24657712..24660361,2	MCF-7	breast:
29	chr14:24631619..24637585-chr14:24644952..24647499,6	K562	blood:
30	chr14:24657642..24658319-chrX:77359719..77360284,2	Hela-S3	cervix:
31	chr14:24655837..24658282-chr14:24904503..24906148,2	K562	blood:
32	chr14:24658044..24659944-chr14:24736263..24737980,2	MCF-7	breast:
33	chr1:149223792..149225481-chr14:24649536..24651486,2	MCF-7	breast:
34	chr14:24644916..24647133-chr14:24681211..24683281,2	MCF-7	breast:
35	chr14:24655775..24658265-chr14:24801236..24803229,2	MCF-7	breast:
36	chr14:24647373..24649581-chr14:24682421..24684138,2	MCF-7	breast:
37	chr14:24631879..24637788-chr14:24639506..24644553,5	K562	blood:
38	chr14:24655120..24666858-chr14:24765577..24776253,24	MCF-7	breast:
39	chr14:24656467..24658398-chr14:24732926..24735303,2	MCF-7	breast:
40	chr14:24633156..24635332-chr14:24644913..24646452,2	K562	blood:
41	chr14:24629462..24633065-chr14:24656618..24659351,3	K562	blood:
42	chr14:24634478..24636921-chr14:24656618..24658137,2	K562	blood:
43	chr14:24549877..24552105-chr14:24657593..24659163,2	MCF-7	breast:
44	chr11:65686028..65688370-chr14:24657521..24659456,2	MCF-7	breast:
45	chr14:24639747..24642550-chr14:24651922..24653711,2	K562	blood:
46	chr14:24634103..24636921-chr14:24656610..24658137,3	K562	blood:
47	chr14:24651928..24654736-chr14:24673769..24676692,2	MCF-7	breast:
48	chr14:24616879..24619569-chr14:24649212..24652143,2	K562	blood:
49	chr14:24658118..24660026-chr14:24704651..24707392,2	MCF-7	breast:
50	chr14:24625193..24627577-chr14:24641996..24645426,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHMP4A-1	chr14:24651818-24651906	l_944_chr14:24641101-24695318_testes
2	lnc-REC8-1	chr14:24651818-24651906	l_943_chr14:24634326-24661062_testes
3	lnc-RP11-468E2.4.1-2	chr14:24646716-24646747	NONHSAT035999
4	lnc-RP11-468E2.4.1-2	chr14:24646915-24647306	NONHSAT035999
5	lnc-REC8-1	chr14:24660129-24660182	l_943_chr14:24634326-24661062_testes

No data

Variant related genes	Relation type
IPO4	TF binding region
ENSG00000259522	TF binding region
REC8	TF binding region
IPO4	CpG island
ENSG00000259522	CpG island
REC8	CpG island
ENSG00000157379	chromatin interactions
ENSG00000136305	chromatin interactions
ENSG00000139914	chromatin interactions
ENSG00000259431	chromatin interactions
ENSG00000268702	chromatin interactions
ENSG00000269955	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000213928	chromatin interactions
ENSG00000175550	chromatin interactions
ENSG00000100911	chromatin interactions
ENSG00000100918	chromatin interactions
ENSG00000213920	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000100836	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000196497	chromatin interactions
ENSG00000129559	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000102144	chromatin interactions
ENSG00000100938	chromatin interactions
ENSG00000238279	chromatin interactions
ENSG00000139908	chromatin interactions
ENSG00000213903	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000213983	chromatin interactions
ENSG00000260669	chromatin interactions
ENSG00000213906	chromatin interactions
ENSG00000172893	chromatin interactions
ENSG00000092295	chromatin interactions
ENSG00000129467	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000092010	chromatin interactions
ENSG00000100949	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000255526	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000092098	chromatin interactions

Extended variants
information (count: 974 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547015980	chr14:24642805-24642806	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs367687356	chr14:24642818-24642819	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs142003521	chr14:24642969-24642970	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs534412182	chr14:24642970-24642971	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs138846376	chr14:24642992-24642993	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs7154911	chr14:24643025-24643026	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs538194965	chr14:24643052-24643053	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs200193934	chr14:24643060-24643061	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs374748944	chr14:24643074-24643075	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs556815498	chr14:24643075-24643076	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs552268017	chr14:24643086-24643087	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs569079829	chr14:24643095-24643096	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs538051722	chr14:24643132-24643133	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs111784995	chr14:24643165-24643166	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs554955709	chr14:24643168-24643169	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs568783385	chr14:24643213-24643214	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs533533295	chr14:24643215-24643216	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs577620036	chr14:24643285-24643286	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs534852363	chr14:24643295-24643296	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs553765803	chr14:24643296-24643297	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs576932782	chr14:24643335-24643336	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs544963667	chr14:24643367-24643368	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs6573596	chr14:24643393-24643394	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs576261927	chr14:24643412-24643413	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs370452592	chr14:24643413-24643414	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs182087873	chr14:24643418-24643419	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs186605795	chr14:24643472-24643473	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs192412954	chr14:24643473-24643474	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs540247761	chr14:24643482-24643483	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs183843146	chr14:24643549-24643550	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs375031164	chr14:24643611-24643612	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs369122913	chr14:24643711-24643712	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs572179437	chr14:24643712-24643713	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs8019327	chr14:24643733-24643734	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372780149	chr14:24643734-24643735	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs561768897	chr14:24643780-24643781	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs1998424	chr14:24643782-24643783	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs560976348	chr14:24643791-24643792	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs66645687	chr14:24643799-24643800	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs540266105	chr14:24643801-24643802	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs146346431	chr14:24643814-24643815	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs568645649	chr14:24643835-24643836	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs188807741	chr14:24643839-24643840	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs547799260	chr14:24643859-24643860	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs66612000	chr14:24643903-24643904	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs544181520	chr14:24644027-24644028	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs4981495	chr14:24644109-24644110	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545302158	chr14:24644138-24644139	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs138194479	chr14:24644149-24644150	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs192818919	chr14:24644172-24644173	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1200 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24631600-24653800	Weak transcription	K562	blood
2	chr14:24635200-24647400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr14:24635400-24647800	Weak transcription	HMEC	breast
4	chr14:24635600-24647000	Weak transcription	Dnd41	blood
5	chr14:24636200-24646000	Weak transcription	Stomach Mucosa	stomach
6	chr14:24636600-24646000	Weak transcription	Small Intestine	intestine
7	chr14:24636600-24647400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr14:24637000-24648000	Weak transcription	HSMM	muscle
9	chr14:24637000-24648200	Weak transcription	HSMMtube	muscle
10	chr14:24637200-24644400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr14:24637200-24645800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:24637200-24645800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:24637200-24646000	Weak transcription	HepG2	liver
14	chr14:24637200-24648000	Weak transcription	Aorta	Aorta
15	chr14:24638200-24648600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:24638200-24648600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr14:24638800-24643800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:24639200-24645800	Weak transcription	Osteobl	bone
19	chr14:24640200-24642800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:24640800-24642800	Strong transcription	NHLF	lung
21	chr14:24641200-24645800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr14:24641200-24647800	Strong transcription	Liver	Liver
23	chr14:24641400-24642800	Strong transcription	NHEK	skin
24	chr14:24641400-24643000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
25	chr14:24641400-24647600	Weak transcription	Psoas Muscle	Psoas
26	chr14:24641400-24648200	Weak transcription	Left Ventricle	heart
27	chr14:24641400-24656000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:24641600-24642800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr14:24641600-24642800	Strong transcription	Colonic Mucosa	Colon
30	chr14:24641600-24642800	Strong transcription	Duodenum Mucosa	Duodenum
31	chr14:24641600-24642800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
32	chr14:24641600-24644600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr14:24641600-24646000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr14:24641600-24646000	Weak transcription	Ovary	ovary
35	chr14:24641600-24646200	Weak transcription	Esophagus	oesophagus
36	chr14:24641600-24648400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:24641600-24648600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr14:24641600-24656600	Strong transcription	Placenta	Placenta
39	chr14:24641600-24656800	Weak transcription	Right Atrium	heart
40	chr14:24641800-24642800	Weak transcription	Primary T cells from cord blood	blood
41	chr14:24641800-24643000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:24641800-24644000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:24641800-24644600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr14:24641800-24645800	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr14:24641800-24646000	Weak transcription	Colon Smooth Muscle	Colon
46	chr14:24641800-24646200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr14:24641800-24647800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr14:24641800-24648000	Weak transcription	NHDF-Ad	bronchial
49	chr14:24641800-24649600	Weak transcription	HUVEC	blood vessel
50	chr14:24641800-24653400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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