Variant report

Variant	nsv482171
Chromosome Location	chr14:24908974-24912007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:729)
CpG islands
(count:305)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24911425-24912397	HepG2	liver:	n/a	n/a
2	ATF1	chr14:24911787-24912300	K562	blood:	n/a	n/a
3	ATF2	chr14:24911650-24912348	GM12878	blood:	n/a	n/a
4	ATF2	chr14:24911370-24912110	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr14:24911439-24912414	GM12878	blood:	n/a	n/a
6	ATF3	chr14:24911349-24911776	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr14:24911877-24912196	K562	blood:	n/a	n/a
8	BACH1	chr14:24911594-24912419	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr14:24911713-24912180	GM12878	blood:	n/a	n/a
10	BCL3	chr14:24911454-24912316	A549	lung:	n/a	n/a
11	BCL3	chr14:24910948-24912407	A549	lung:	n/a	n/a
12	BCLAF1	chr14:24912000-24912419	K562	blood:	n/a	n/a
13	BCLAF1	chr14:24911184-24912431	GM12878	blood:	n/a	n/a
14	BCLAF1	chr14:24911651-24912552	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:24911242-24912270	HepG2	liver:	n/a	n/a
16	BHLHE40	chr14:24911419-24912438	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:24911459-24912295	K562	blood:	n/a	n/a
18	BRCA1	chr14:24911444-24912268	HepG2	liver:	n/a	n/a
19	BRCA1	chr14:24911441-24912353	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr14:24911652-24911849	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr14:24911317-24912402	K562	blood:	n/a	n/a
22	CCNT2	chr14:24911894-24912299	K562	blood:	n/a	n/a
23	CCNT2	chr14:24911369-24911655	K562	blood:	n/a	n/a
24	CEBPB	chr14:24911583-24912287	IMR90	lung:	n/a	n/a
25	CEBPB	chr14:24911710-24912303	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:24911884-24912335	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr14:24911917-24912286	A549	lung:	n/a	n/a
28	CEBPB	chr14:24911902-24912220	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:24911243-24912356	MCF-7	breast:	n/a	n/a
30	CEBPB	chr14:24911816-24912379	A549	lung:	n/a	n/a
31	CEBPB	chr14:24911840-24912320	K562	blood:	n/a	n/a
32	CEBPB	chr14:24911735-24912301	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:24911346-24912309	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:24911902-24912271	A549	lung:	n/a	n/a
35	CEBPB	chr14:24911480-24912389	HepG2	liver:	n/a	n/a
36	CEBPB	chr14:24911885-24912288	K562	blood:	n/a	n/a
37	CEBPB	chr14:24911447-24912345	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr14:24911503-24912451	GM12878	blood:	n/a	n/a
39	CEBPD	chr14:24911091-24912443	HepG2	liver:	n/a	n/a
40	CEBPD	chr14:24911190-24912393	HepG2	liver:	n/a	n/a
41	CHD1	chr14:24911486-24912570	GM12878	blood:	n/a	n/a
42	CHD1	chr14:24910986-24912822	IMR90	lung:	n/a	n/a
43	CHD1	chr14:24911534-24911894	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr14:24911143-24912361	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr14:24911547-24912358	GM12878	blood:	n/a	n/a
46	CHD2	chr14:24911347-24912300	HepG2	liver:	n/a	n/a
47	CHD2	chr14:24911676-24912257	K562	blood:	n/a	n/a
48	CHD2	chr14:24911115-24912371	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr14:24911349-24912262	A549	lung:	n/a	n/a
50	CREB1	chr14:24911415-24911722	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24911653-24911703	AG04450	lung:	fetal
2	chr14:24911653-24911703	AG04449	skin:	fetal
3	chr14:24911994-24912044	SK-N-MC	brain:	n/a
4	chr14:24911839-24911889	IMR90	lung:	fetal
5	chr14:24911994-24912044	BJ	skin:	n/a
6	chr14:24911599-24911649	Hela-S3	cervix:	n/a
7	chr14:24911599-24911649	A549	lung:	n/a
8	chr14:24911599-24911649	HEEpiC	esophagus:	n/a
9	chr14:24911653-24911703	NHBE	bronchial:	n/a
10	chr14:24911839-24911889	Caco-2	colon:	n/a
11	chr14:24911653-24911703	HCPEpiC	choroid plexus:	n/a
12	chr14:24911839-24911889	GM12878	blood:	n/a
13	chr14:24911839-24911889	A549	lung:	n/a
14	chr14:24911599-24911649	HNPCEpiC	eye:	n/a
15	chr14:24909125-24909175	HCM	heart:	n/a
16	chr14:24909125-24909175	Hela-S3	cervix:	n/a
17	chr14:24911994-24912044	GM12891	blood:	n/a
18	chr14:24909125-24909175	AG04450	lung:	fetal
19	chr14:24911994-24912044	Hepatocyte	liver:	n/a
20	chr14:24911839-24911889	HRCEpiC	kidney:	n/a
21	chr14:24911839-24911889	ECC-1	luminal epithelium:	n/a
22	chr14:24911994-24912044	NHDF-neo	bronchial:	n/a
23	chr14:24911653-24911703	H1-hESC	embryonic stem cell:	embryo
24	chr14:24911994-24912044	BE2_C	brain:	n/a
25	chr14:24911839-24911889	HUVEC	blood vessel:	n/a
26	chr14:24911653-24911703	K562	blood:	n/a
27	chr14:24911839-24911889	HEK293	kidney:	embryo
28	chr14:24911839-24911889	HCPEpiC	choroid plexus:	n/a
29	chr14:24911839-24911889	Hela-S3	cervix:	n/a
30	chr14:24911839-24911889	AG09319	gingival:	n/a
31	chr14:24911653-24911703	NB4	blood:	n/a
32	chr14:24911599-24911649	ECC-1	luminal epithelium:	n/a
33	chr14:24911839-24911889	GM19239	blood:	n/a
34	chr14:24909125-24909175	GM19239	blood:	n/a
35	chr14:24911653-24911703	MCF10A-Er-Src	breast:	n/a
36	chr14:24909125-24909175	HNPCEpiC	eye:	n/a
37	chr14:24909125-24909175	HEK293	kidney:	embryo
38	chr14:24911994-24912044	HL-60	blood:	n/a
39	chr14:24911839-24911889	ovcar-3	ovarian:	n/a
40	chr14:24909125-24909175	NB4	blood:	n/a
41	chr14:24911599-24911649	IMR90	lung:	fetal
42	chr14:24911653-24911703	BJ	skin:	n/a
43	chr14:24911599-24911649	HPAEpiC	pulmonary alveolar:	n/a
44	chr14:24911839-24911889	GM06990	blood:	n/a
45	chr14:24909125-24909175	HL-60	blood:	n/a
46	chr14:24911599-24911649	Jurkat	blood:	n/a
47	chr14:24911994-24912044	CMK	blood:	n/a
48	chr14:24911994-24912044	HUVEC	blood vessel:	n/a
49	chr14:24911653-24911703	GM19239	blood:	n/a
50	chr14:24909125-24909175	HRPEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24767708..24770495-chr14:24910481..24913051,4	MCF-7	breast:
2	chr14:24911283..24912112-chr6:26123642..26124468,2	Hela-S3	cervix:
3	chr14:24801605..24806320-chr14:24904693..24909744,5	K562	blood:
4	chr14:24909091..24910881-chr4:187644537..187646251,2	MCF-7	breast:
5	chr11:57435097..57435828-chr14:24911287..24912136,2	Hela-S3	cervix:
6	chr14:24796552..24799266-chr14:24908909..24911628,3	K562	blood:
7	chr14:24709335..24712189-chr14:24910783..24914037,3	K562	blood:
8	chr10:70715820..70716456-chr14:24911635..24912197,2	Hela-S3	cervix:
9	chr14:24783396..24785005-chr14:24908424..24911111,2	K562	blood:
10	chr14:24827418..24850855-chr14:24894884..24913772,127	MCF-7	breast:
11	chr14:24872891..24878220-chr14:24906746..24909504,4	MCF-7	breast:
12	chr14:24911126..24911967-chr19:17829461..17830386,2	Hela-S3	cervix:
13	chr14:24816528..24849574-chr14:24893305..24914155,145	MCF-7	breast:
14	chr14:24860779..24862341-chr14:24908273..24910091,2	MCF-7	breast:
15	chr14:24791358..24808812-chr14:24895309..24913599,55	K562	blood:
16	chr14:24738849..24740758-chr14:24911753..24913964,2	MCF-7	breast:
17	chr1:28907885..28908389-chr14:24911165..24911955,2	Hela-S3	cervix:
18	chr14:24738558..24740532-chr14:24907754..24910468,2	MCF-7	breast:
19	chr14:24698279..24701346-chr14:24909291..24912292,3	MCF-7	breast:
20	chr14:24911539..24912418-chr16:9185072..9185743,2	Hela-S3	cervix:
21	chr14:24774877..24777510-chr14:24906503..24909154,3	MCF-7	breast:
22	chr14:24898746..24899612-chr14:24911431..24912345,3	Hela-S3	cervix:
23	chr14:24781460..24810019-chr14:24892340..24914262,110	MCF-7	breast:
24	chr14:24911438..24912197-chr19:50379665..50380613,2	Hela-S3	cervix:
25	chr14:24911102..24911676-chr2:101924903..101925680,2	Hela-S3	cervix:
26	chr1:32687998..32688525-chr14:24911489..24912001,2	HCT-116	colon:
27	chr14:24800598..24804207-chr14:24909756..24912911,5	K562	blood:
28	chr14:24911390..24911912-chr18:3447089..3447840,2	Hela-S3	cervix:
29	chr14:24911211..24912178-chr19:13875300..13875832,2	Hela-S3	cervix:
30	chr12:49524736..49525428-chr14:24911238..24912051,2	Hela-S3	cervix:
31	chr14:24836714..24839783-chr14:24910555..24913487,3	K562	blood:
32	chr14:24767332..24771774-chr14:24910139..24913002,7	MCF-7	breast:
33	chr14:24911320..24912101-chr6:24720852..24721499,2	Hela-S3	cervix:
34	chr14:24910782..24911552-chr4:71858996..71859672,2	Hela-S3	cervix:
35	chr11:61582689..61583740-chr14:24911655..24912354,3	Hela-S3	cervix:
36	chr14:24789439..24822082-chr14:24898039..24913135,99	MCF-7	breast:
37	chr14:24562331..24564529-chr14:24910345..24912043,2	K562	blood:
38	chr14:24909605..24912144-chr17:56736218..56737898,2	MCF-7	breast:
39	chr12:7053057..7053838-chr14:24911391..24912053,2	Hela-S3	cervix:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SDR39U1	hsa-miR-1	chr14:24909050-24909072

Variant related genes	Relation type
SDR39U1	TF binding region
SDR39U1	CpG island
ENSG00000197989	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000165732	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000156599	chromatin interactions
ENSG00000222326	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000204673	chromatin interactions
ENSG00000100949	chromatin interactions
ENSG00000083857	chromatin interactions
ENSG00000213903	chromatin interactions
ENSG00000130479	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000100968	chromatin interactions
ENSG00000156136	chromatin interactions
ENSG00000258973	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000136305	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000163162	chromatin interactions
ENSG00000037757	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000182831	chromatin interactions
ENSG00000213906	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000129465	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000207141	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000129559	chromatin interactions
ENSG00000084623	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000129467	chromatin interactions
ENSG00000177426	chromatin interactions
ENSG00000149485	chromatin interactions

Extended variants
information (count: 147 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:147 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548732126	chr14:24909006-24909007	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs374356443	chr14:24909026-24909027	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs376422559	chr14:24909060-24909061	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region miRNA target site	10 gene(s)	Overlapped CNVs	n/a
4	rs3809	chr14:24909072-24909073	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region miRNA target site	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs551457382	chr14:24909078-24909079	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs571473116	chr14:24909145-24909146	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs537217822	chr14:24909160-24909161	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs550906888	chr14:24909173-24909174	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs567597804	chr14:24909224-24909225	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs62000699	chr14:24909237-24909238	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs1043839	chr14:24909281-24909282	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs200384606	chr14:24909290-24909291	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs200170657	chr14:24909305-24909306	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs534816937	chr14:24909345-24909346	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs557782219	chr14:24909359-24909360	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs1043831	chr14:24909362-24909363	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs17844876	chr14:24909363-24909364	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs367826860	chr14:24909384-24909385	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs370095605	chr14:24909396-24909397	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs7159891	chr14:24909400-24909401	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574298180	chr14:24909402-24909403	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs368549753	chr14:24909407-24909408	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs188940530	chr14:24909408-24909409	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs372475511	chr14:24909411-24909412	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs375422080	chr14:24909432-24909433	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs7157920	chr14:24909436-24909437	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs371901244	chr14:24909441-24909442	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs35580864	chr14:24909458-24909459	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs368937577	chr14:24909469-24909470	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs181549511	chr14:24909474-24909475	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs3211056	chr14:24909475-24909476	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs17849387	chr14:24909476-24909477	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs201366392	chr14:24909501-24909502	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs369769186	chr14:24909514-24909515	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs541216462	chr14:24909534-24909535	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs373640189	chr14:24909535-24909536	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs200984811	chr14:24909584-24909585	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs201633979	chr14:24909585-24909586	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs201317227	chr14:24909586-24909587	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs200399285	chr14:24909588-24909589	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs200019701	chr14:24909621-24909622	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs546834265	chr14:24909624-24909625	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs11538256	chr14:24909629-24909630	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs200225837	chr14:24909630-24909631	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs370209428	chr14:24909635-24909636	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs373631253	chr14:24909644-24909645	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs534989024	chr14:24909655-24909656	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs376443762	chr14:24909659-24909660	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs557845473	chr14:24909683-24909684	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs571435042	chr14:24909729-24909730	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24900200-24911000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:24900600-24910600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:24901400-24910200	Strong transcription	Aorta	Aorta
4	chr14:24901600-24909800	Weak transcription	Fetal Heart	heart
5	chr14:24901600-24910400	Strong transcription	Placenta Amnion	Placenta Amnion
6	chr14:24901800-24909000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:24901800-24910000	Strong transcription	Sigmoid Colon	Sigmoid Colon
8	chr14:24902000-24909200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:24902200-24909400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr14:24902400-24909400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr14:24902400-24909800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:24902400-24910200	Strong transcription	A549	lung
13	chr14:24902400-24910600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:24903000-24910000	Weak transcription	Psoas Muscle	Psoas
15	chr14:24903000-24910000	Strong transcription	NHEK	skin
16	chr14:24903400-24909600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:24903800-24909000	Strong transcription	Pancreas	Pancrea
18	chr14:24904200-24910200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
19	chr14:24904400-24910400	Genic enhancers	Adipose Nuclei	Adipose
20	chr14:24904600-24910400	Strong transcription	Fetal Lung	lung
21	chr14:24904800-24910400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:24905400-24910000	Genic enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:24905400-24910600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:24905400-24910600	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr14:24905400-24911000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr14:24905800-24910600	Strong transcription	HSMM	muscle
27	chr14:24906000-24909200	Strong transcription	NH-A	brain
28	chr14:24906000-24909200	Strong transcription	NHLF	lung
29	chr14:24906000-24909400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:24906000-24909400	Strong transcription	Muscle Satellite Cultured Cells	--
31	chr14:24906000-24910000	Strong transcription	Fetal Intestine Small	intestine
32	chr14:24906000-24910200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:24906000-24910400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr14:24906000-24910400	Strong transcription	Osteobl	bone
35	chr14:24906200-24909400	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr14:24906200-24909800	Strong transcription	HepG2	liver
37	chr14:24906200-24910400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:24906200-24910400	Genic enhancers	Spleen	Spleen
39	chr14:24906200-24910600	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr14:24906400-24909000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr14:24906400-24909400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:24906400-24909600	Strong transcription	Brain Angular Gyrus	brain
43	chr14:24906400-24909800	Strong transcription	Brain Cingulate Gyrus	brain
44	chr14:24906400-24909800	Strong transcription	Brain Substantia Nigra	brain
45	chr14:24906400-24909800	Strong transcription	Fetal Intestine Large	intestine
46	chr14:24906400-24910200	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr14:24906400-24910400	Strong transcription	Rectal Smooth Muscle	rectum
48	chr14:24906400-24910600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr14:24906600-24909000	Strong transcription	Brain Inferior Temporal Lobe	brain
50	chr14:24906600-24909200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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