Variant report

Variant	esv3528012
Chromosome Location	chr14:105260807-105263255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:105262944-105262977	K562	blood:	n/a	n/a
2	BACH1	chr14:105261472-105261498	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:105262155-105262338	K562	blood:	n/a	n/a
4	BHLHE40	chr14:105262625-105263043	HepG2	liver:	n/a	n/a
5	BRCA1	chr14:105262685-105262843	HepG2	liver:	n/a	n/a
6	BRCA1	chr14:105262304-105262403	GM12878	blood:	n/a	n/a
7	CCNT2	chr14:105261098-105262537	K562	blood:	n/a	n/a
8	CHD1	chr14:105262711-105262801	GM12878	blood:	n/a	n/a
9	CHD1	chr14:105262284-105262391	GM12878	blood:	n/a	n/a
10	CHD1	chr14:105261172-105261559	GM12878	blood:	n/a	n/a
11	CHD2	chr14:105262235-105262645	GM12878	blood:	n/a	n/a
12	CHD2	chr14:105262648-105263144	K562	blood:	n/a	n/a
13	CHD2	chr14:105262807-105263055	HepG2	liver:	n/a	n/a
14	CHD2	chr14:105262067-105262253	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr14:105260642-105260849	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr14:105262961-105263123	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr14:105261136-105261230	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr14:105261016-105261458	GM12878	blood:	n/a	n/a
19	CREB1	chr14:105261978-105262243	A549	lung:	n/a	n/a
20	CREB1	chr14:105260318-105260899	HepG2	liver:	n/a	n/a
21	CTCF	chr14:105261082-105261234	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:105261090-105261210	HepG2	liver:	n/a	n/a
23	CTCF	chr14:105261200-105261350	GM12864	blood:	n/a	n/a
24	CTCF	chr14:105261100-105261250	GM06990	blood:	n/a	n/a
25	CTCF	chr14:105261113-105261219	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr14:105261000-105261150	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr14:105260960-105261110	HPF	lung:	n/a	n/a
28	CTCF	chr14:105261080-105261230	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr14:105261140-105261290	HVMF	connective:	n/a	n/a
30	CTCF	chr14:105261143-105261147	GM13977	blood:	n/a	n/a
31	CTCF	chr14:105260980-105261287	GM12878	blood:	n/a	n/a
32	CTCF	chr14:105261091-105261215	ProgFib	skin:	n/a	n/a
33	CTCF	chr14:105261036-105261216	HepG2	liver:	n/a	n/a
34	CTCF	chr14:105261106-105261108	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr14:105261020-105261170	AG09319	gingival:	n/a	n/a
36	CTCF	chr14:105261125-105261196	A549	lung:	n/a	n/a
37	CTCF	chr14:105261051-105261274	GM12892	blood:	n/a	n/a
38	CTCF	chr14:105261080-105261230	NHEK	skin:	n/a	n/a
39	CTCF	chr14:105263060-105263210	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr14:105261140-105261290	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr14:105261129-105261248	GM12878	blood:	n/a	n/a
42	CTCF	chr14:105261200-105261350	A549	lung:	n/a	n/a
43	CTCF	chr14:105261060-105261210	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr14:105261144-105261195	NHEK	skin:	n/a	n/a
45	CTCF	chr14:105261020-105261170	GM12872	blood:	n/a	n/a
46	CTCF	chr14:105261020-105261170	HFF	foreskin:	n/a	n/a
47	CTCF	chr14:105261020-105261170	HMF	breast:	n/a	n/a
48	CTCF	chr14:105261060-105261210	HepG2	liver:	n/a	n/a
49	CTCF	chr14:105261091-105261224	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:105261050-105261154	Pancreas_OC	pancreas:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105263191-105263241	MCF10A-Er-Src	breast:	n/a
2	chr14:105263191-105263241	MCF10A-Er-Src	breast:	n/a
3	chr14:105261564-105261614	AG04449	skin:	fetal
4	chr14:105261335-105261385	NHDF-neo	bronchial:	n/a
5	chr14:105261335-105261385	AG09319	gingival:	n/a
6	chr14:105263191-105263241	HCM	heart:	n/a
7	chr14:105262406-105262456	GM12891	blood:	n/a
8	chr14:105262276-105262326	BE2_C	brain:	n/a
9	chr14:105262406-105262456	AG04450	lung:	fetal
10	chr14:105261564-105261614	GM06990	blood:	n/a
11	chr14:105261564-105261614	NB4	blood:	n/a
12	chr14:105262269-105262319	LNCaP	prostate:	n/a
13	chr14:105263191-105263241	GM19239	blood:	n/a
14	chr14:105263191-105263241	HCT-116	colon:	n/a
15	chr14:105261335-105261385	RPTEC	kidney:	n/a
16	chr14:105262305-105262355	HNPCEpiC	eye:	n/a
17	chr14:105262348-105262398	SK-N-SH	brain:	n/a
18	chr14:105262269-105262319	HCF	heart:	n/a
19	chr14:105263191-105263241	GM12891	blood:	n/a
20	chr14:105263191-105263241	SK-N-MC	brain:	n/a
21	chr14:105262406-105262456	HAEpiC	amniotic membrane:	n/a
22	chr14:105261564-105261614	AG09319	gingival:	n/a
23	chr14:105261335-105261385	NB4	blood:	n/a
24	chr14:105261335-105261385	Hela-S3	cervix:	n/a
25	chr14:105262276-105262326	AG04450	lung:	fetal
26	chr14:105261564-105261614	Hepatocyte	liver:	n/a
27	chr14:105262305-105262355	MCF10A-Er-Src	breast:	n/a
28	chr14:105262406-105262456	LNCaP	prostate:	n/a
29	chr14:105262276-105262326	LNCaP	prostate:	n/a
30	chr14:105262276-105262326	SK-N-SH_RA	brain:	n/a
31	chr14:105262269-105262319	U87	brain:	n/a
32	chr14:105262406-105262456	PANC-1	pancreas:	n/a
33	chr14:105261564-105261614	H1-hESC	embryonic stem cell:	embryo
34	chr14:105262406-105262456	HEEpiC	esophagus:	n/a
35	chr14:105262305-105262355	GM19239	blood:	n/a
36	chr14:105262406-105262456	BJ	skin:	n/a
37	chr14:105261564-105261614	MCF-7	breast:	n/a
38	chr14:105261335-105261385	A549	lung:	n/a
39	chr14:105262305-105262355	GM12878	blood:	n/a
40	chr14:105263191-105263241	ovcar-3	ovarian:	n/a
41	chr14:105263191-105263241	HepG2	liver:	n/a
42	chr14:105262305-105262355	SK-N-SH_RA	brain:	n/a
43	chr14:105261564-105261614	Hela-S3	cervix:	n/a
44	chr14:105262406-105262456	H1-hESC	embryonic stem cell:	embryo
45	chr14:105262276-105262326	T-47D	breast:	n/a
46	chr14:105262276-105262326	SAEC	small airway:	n/a
47	chr14:105262406-105262456	AG04449	skin:	fetal
48	chr14:105262276-105262326	HepG2	liver:	n/a
49	chr14:105262348-105262398	HCM	heart:	n/a
50	chr14:105262276-105262326	Hela-S3	cervix:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105261442..105265036-chr14:105329931..105332556,6	MCF-7	breast:
2	chr14:105188879..105190553-chr14:105260910..105263562,2	MCF-7	breast:
3	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
4	chr14:105190071..105193724-chr14:105262102..105266779,4	K562	blood:
5	chr14:105260251..105263637-chr14:105331262..105334523,4	K562	blood:
6	chr10:102825608..102826586-chr14:105261508..105262019,2	Hela-S3	cervix:
7	chr14:105219293..105222032-chr14:105260458..105263797,3	MCF-7	breast:
8	chr14:105260375..105263562-chr14:105329763..105332955,5	MCF-7	breast:
9	chr14:105189251..105191715-chr14:105260176..105263336,3	MCF-7	breast:
10	chr14:105145208..105149817-chr14:105259856..105263393,4	MCF-7	breast:
11	chr1:153643198..153643841-chr14:105262172..105262866,2	Hela-S3	cervix:
12	chr14:105234268..105237912-chr14:105260331..105262677,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHNAK2-7	chr14:105261348-105261381	NONHSAT040280

No data

Variant related genes	Relation type
ZBTB42	TF binding region
AKT1	TF binding region
ZBTB42	CpG island
AKT1	CpG island
ENSG00000185100	chromatin interactions
ENSG00000184990	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000143621	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000107821	chromatin interactions
ENSG00000258430	chromatin interactions
ENSG00000256050	chromatin interactions

Extended variants
information (count: 59 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:59 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529626374	chr14:105260828-105260829	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs549290087	chr14:105260857-105260858	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs78837721	chr14:105260898-105260899	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs72522810	chr14:105260905-105260906	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs61757055	chr14:105260906-105260907	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs200395565	chr14:105260907-105260908	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs200808987	chr14:105260911-105260912	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs566310261	chr14:105260950-105260951	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs528556915	chr14:105260969-105260970	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs551413840	chr14:105260996-105260997	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs571428731	chr14:105261037-105261038	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs569368816	chr14:105261105-105261106	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs117096287	chr14:105261123-105261124	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs547234181	chr14:105261135-105261136	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs556970472	chr14:105261174-105261175	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs567423597	chr14:105261193-105261194	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs565873572	chr14:105261198-105261199	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs552880465	chr14:105261330-105261331	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs36214921	chr14:105261414-105261415	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs10144641	chr14:105261419-105261420	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs558659108	chr14:105261529-105261530	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs200512697	chr14:105262025-105262026	Weak transcription Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs575429386	chr14:105262041-105262042	Weak transcription Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs3002448	chr14:105262042-105262043	Weak transcription Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs192433222	chr14:105262309-105262310	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs376844098	chr14:105262350-105262351	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs534197838	chr14:105262360-105262361	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs2498786	chr14:105262368-105262369	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543348675	chr14:105262441-105262442	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs559806193	chr14:105262446-105262447	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs183769910	chr14:105262476-105262477	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs551571963	chr14:105262591-105262592	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs530000363	chr14:105262624-105262625	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs71129248	chr14:105262664-105262665	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs565020326	chr14:105262691-105262692	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs530937526	chr14:105262701-105262702	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs550696024	chr14:105262763-105262764	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs74090038	chr14:105262781-105262782	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113973378	chr14:105262805-105262806	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs546824339	chr14:105262822-105262823	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs539648992	chr14:105262836-105262837	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs28546406	chr14:105262845-105262846	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs188840784	chr14:105262847-105262848	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs117316489	chr14:105262859-105262860	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs558822359	chr14:105262860-105262861	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs2494750	chr14:105262912-105262913	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs537988624	chr14:105262934-105262935	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs2494751	chr14:105262961-105262962	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574337151	chr14:105262976-105262977	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs539867552	chr14:105262995-105262996	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105258800-105261200	Flanking Active TSS	Liver	Liver
2	chr14:105258800-105261200	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr14:105259000-105261200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr14:105259000-105261400	Flanking Active TSS	Stomach Smooth Muscle	stomach
5	chr14:105259400-105261200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr14:105259600-105261000	Flanking Active TSS	GM12878-XiMat	blood
7	chr14:105259800-105261000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
8	chr14:105259800-105261000	Flanking Active TSS	Rectal Smooth Muscle	rectum
9	chr14:105259800-105261000	Flanking Active TSS	Osteobl	bone
10	chr14:105259800-105261200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:105259800-105261200	Flanking Active TSS	Colon Smooth Muscle	Colon
12	chr14:105259800-105261200	Flanking Active TSS	Hela-S3	cervix
13	chr14:105259800-105261400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr14:105260000-105261000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr14:105260000-105261200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:105260000-105261200	Flanking Active TSS	Colonic Mucosa	Colon
17	chr14:105260000-105261200	Flanking Active TSS	Duodenum Mucosa	Duodenum
18	chr14:105260000-105261200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr14:105260000-105261200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr14:105260000-105261200	Flanking Active TSS	NH-A	brain
21	chr14:105260000-105261400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr14:105260000-105261400	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr14:105260000-105261400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr14:105260200-105261000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:105260200-105261000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr14:105260200-105261000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr14:105260200-105261000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr14:105260200-105261000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
29	chr14:105260200-105261000	Flanking Active TSS	HMEC	breast
30	chr14:105260200-105261000	Flanking Active TSS	HUVEC	blood vessel
31	chr14:105260200-105261200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:105260200-105261200	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr14:105260200-105261200	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr14:105260200-105261200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr14:105260200-105261200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr14:105260200-105261200	Flanking Active TSS	K562	blood
37	chr14:105260200-105261400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr14:105260200-105261400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:105260200-105261400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr14:105260200-105261400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr14:105260200-105261400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:105260200-105261400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr14:105260200-105261400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr14:105260200-105261400	Flanking Active TSS	Right Ventricle	heart
45	chr14:105260200-105261400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr14:105260200-105261600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr14:105260200-105262600	Active TSS	H9 Cell Line	embryonic stem cell
48	chr14:105260400-105261000	Flanking Active TSS	NHEK	skin
49	chr14:105260400-105261200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr14:105260400-105261200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood

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