Variant report

Variant	esv34146
Chromosome Location	chr5:115315944-115729919
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3174)
CpG islands
(count:2016)
Chromatin interactive
region (count:132)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3174 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115367900-115368175	K562	blood:	n/a	n/a
2	ARID3A	chr5:115567073-115567351	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:115338438-115338492	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:115410898-115411078	K562	blood:	n/a	n/a
5	ARID3A	chr5:115420453-115420725	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:115403795-115404079	K562	blood:	n/a	n/a
7	ARID3A	chr5:115473442-115473811	K562	blood:	n/a	n/a
8	ARID3A	chr5:115420927-115421286	HepG2	liver:	n/a	n/a
9	ATF1	chr5:115707706-115707979	K562	blood:	n/a	n/a
10	ATF1	chr5:115679669-115679868	K562	blood:	n/a	n/a
11	ATF1	chr5:115367730-115368219	K562	blood:	n/a	n/a
12	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
13	ATF1	chr5:115394162-115394612	K562	blood:	n/a	n/a
14	ATF1	chr5:115700581-115701001	K562	blood:	n/a	n/a
15	ATF1	chr5:115420602-115421231	K562	blood:	n/a	n/a
16	ATF1	chr5:115410893-115411113	K562	blood:	n/a	n/a
17	ATF1	chr5:115705390-115705679	K562	blood:	n/a	n/a
18	ATF1	chr5:115342618-115342831	K562	blood:	n/a	n/a
19	ATF1	chr5:115694484-115694974	K562	blood:	n/a	n/a
20	ATF1	chr5:115426098-115426398	K562	blood:	n/a	n/a
21	ATF2	chr5:115700598-115701276	GM12878	blood:	n/a	n/a
22	ATF2	chr5:115420461-115421375	GM12878	blood:	n/a	n/a
23	ATF2	chr5:115470974-115471521	GM12878	blood:	n/a	n/a
24	ATF2	chr5:115694360-115694992	GM12878	blood:	n/a	n/a
25	ATF2	chr5:115411962-115412753	GM12878	blood:	n/a	n/a
26	ATF2	chr5:115697348-115697730	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr5:115694460-115695182	GM12878	blood:	n/a	n/a
28	ATF2	chr5:115367704-115368194	GM12878	blood:	n/a	n/a
29	ATF2	chr5:115420612-115421281	GM12878	blood:	n/a	n/a
30	ATF2	chr5:115412006-115412690	GM12878	blood:	n/a	n/a
31	ATF2	chr5:115367677-115368276	GM12878	blood:	n/a	n/a
32	ATF3	chr5:115367737-115368181	K562	blood:	n/a	n/a
33	ATF3	chr5:115420907-115421300	K562	blood:	n/a	n/a
34	ATF3	chr5:115367703-115368390	HCT-116	colon:	n/a	n/a
35	ATF3	chr5:115420925-115421272	GM12878	blood:	n/a	n/a
36	ATF3	chr5:115420549-115421037	A549	lung:	n/a	n/a
37	BACH1	chr5:115394268-115394429	K562	blood:	n/a	n/a
38	BACH1	chr5:115679748-115679880	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr5:115420883-115421200	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr5:115573174-115573254	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr5:115697108-115697625	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr5:115372974-115373262	GM12878	blood:	n/a	chr5:115373126-115373136 chr5:115373125-115373136
43	BATF	chr5:115412087-115412508	GM12878	blood:	n/a	n/a
44	BATF	chr5:115708897-115709253	GM12878	blood:	n/a	chr5:115709039-115709049 chr5:115709038-115709049
45	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
46	BATF	chr5:115372991-115373241	GM12878	blood:	n/a	chr5:115373126-115373136 chr5:115373125-115373136
47	BATF	chr5:115700697-115701341	GM12878	blood:	n/a	chr5:115700750-115700759
48	BATF	chr5:115411990-115412543	GM12878	blood:	n/a	n/a
49	BATF	chr5:115316893-115317171	GM12878	blood:	n/a	n/a
50	BATF	chr5:115694520-115694822	GM12878	blood:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115418530-115418580	HRCEpiC	kidney:	n/a
2	chr5:115420544-115420594	HNPCEpiC	eye:	n/a
3	chr5:115697370-115697420	HCF	heart:	n/a
4	chr5:115418530-115418580	HRCEpiC	kidney:	n/a
5	chr5:115420544-115420594	HNPCEpiC	eye:	n/a
6	chr5:115697370-115697420	HCF	heart:	n/a
7	chr5:115387984-115388034	GM12891	blood:	n/a
8	chr5:115421194-115421244	NH-A	brain:	n/a
9	chr5:115420814-115420864	HRE	kidney:	n/a
10	chr5:115420761-115420811	ProgFib	skin:	n/a
11	chr5:115387984-115388034	GM19239	blood:	n/a
12	chr5:115373986-115374036	HCPEpiC	choroid plexus:	n/a
13	chr5:115450589-115450639	HAEpiC	amniotic membrane:	n/a
14	chr5:115697214-115697264	PrEC	prostate:	n/a
15	chr5:115418530-115418580	ovcar-3	ovarian:	n/a
16	chr5:115724285-115724335	GM12892	blood:	n/a
17	chr5:115697370-115697420	AG04449	skin:	fetal
18	chr5:115696151-115696201	Hepatocyte	liver:	n/a
19	chr5:115705963-115706013	Jurkat	blood:	n/a
20	chr5:115420761-115420811	SK-N-MC	brain:	n/a
21	chr5:115697214-115697264	GM19239	blood:	n/a
22	chr5:115330940-115330990	SK-N-SH_RA	brain:	n/a
23	chr5:115712252-115712302	Hepatocyte	liver:	n/a
24	chr5:115697446-115697496	HMEC	breast:	n/a
25	chr5:115421035-115421085	HCT-116	colon:	n/a
26	chr5:115387951-115388001	Hepatocyte	liver:	n/a
27	chr5:115420544-115420594	H1-hESC	embryonic stem cell:	embryo
28	chr5:115387951-115388001	A549	lung:	n/a
29	chr5:115697370-115697420	Jurkat	blood:	n/a
30	chr5:115387976-115388026	RPTEC	kidney:	n/a
31	chr5:115421152-115421202	GM12892	blood:	n/a
32	chr5:115697214-115697264	PANC-1	pancreas:	n/a
33	chr5:115697696-115697746	H1-hESC	embryonic stem cell:	embryo
34	chr5:115387951-115388001	NB4	blood:	n/a
35	chr5:115421035-115421085	BJ	skin:	n/a
36	chr5:115639617-115639667	IMR90	lung:	fetal
37	chr5:115367063-115367113	SK-N-SH	brain:	n/a
38	chr5:115420544-115420594	HUVEC	blood vessel:	n/a
39	chr5:115363186-115363236	NHBE	bronchial:	n/a
40	chr5:115322511-115322561	BE2_C	brain:	n/a
41	chr5:115330940-115330990	PFSK-1	brain:	n/a
42	chr5:115418530-115418580	ECC-1	luminal epithelium:	n/a
43	chr5:115712252-115712302	U87	brain:	n/a
44	chr5:115322511-115322561	RPTEC	kidney:	n/a
45	chr5:115373986-115374036	NH-A	brain:	n/a
46	chr5:115421194-115421244	Hepatocyte	liver:	n/a
47	chr5:115639617-115639667	HUVEC	blood vessel:	n/a
48	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:115367063-115367113	Jurkat	blood:	n/a
50	chr5:115419633-115419683	HRCEpiC	kidney:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:114960090..114964183-chr5:115419193..115421485,4	MCF-7	breast:
2	chr5:115325159..115327094-chr5:115327462..115329055,2	K562	blood:
3	chr5:115396887..115398526-chr5:115419327..115421130,2	MCF-7	breast:
4	chr5:115325067..115326852-chr5:115339331..115341155,2	K562	blood:
5	chr5:115175547..115177254-chr5:115379350..115381735,2	MCF-7	breast:
6	chr5:115164592..115166592-chr5:115332938..115334988,2	K562	blood:
7	chr5:115318449..115319995-chr5:115320033..115322882,2	MCF-7	breast:
8	chr4:184425377..184425891-chr5:115420080..115420819,2	Hela-S3	cervix:
9	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
10	chr5:115338156..115340599-chr5:115341199..115344105,2	K562	blood:
11	chr5:115431884..115434416-chr5:115451435..115454225,2	K562	blood:
12	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
13	chr11:21157468..21158972-chr5:115430256..115431756,2	MCF-7	breast:
14	chr5:115409539..115411253-chr5:115413731..115416467,2	K562	blood:
15	chr5:114958936..114960751-chr5:115402229..115404106,2	K562	blood:
16	chr5:115408709..115410572-chr5:115414049..115415857,2	MCF-7	breast:
17	chr5:115223474..115224422-chr5:115405380..115406073,2	MCF-7	breast:
18	chr5:115177392..115178980-chr5:115419410..115421076,2	MCF-7	breast:
19	chr5:115512590..115515778-chr5:115516651..115520258,3	MCF-7	breast:
20	chr5:115355525..115357381-chr5:115358877..115362646,3	MCF-7	breast:
21	chr5:115175649..115178515-chr5:115418843..115420963,3	K562	blood:
22	chr5:115358879..115361762-chr5:115363430..115365377,2	K562	blood:
23	chr5:115418449..115420927-chr5:115462896..115464541,2	K562	blood:
24	chr5:115420835..115421447-chr6:89789827..89790793,2	HCT-116	colon:
25	chr5:115405163..115410303-chr5:115417488..115422793,7	K562	blood:
26	chr5:115477963..115480064-chr5:115480486..115482717,2	K562	blood:
27	chr4:148160683..148161374-chr5:115362795..115363673,2	MCF-7	breast:
28	chr5:115338156..115340599-chr5:115341199..115344105,2	K562	blood:
29	chr5:115325463..115327847-chr5:115335444..115338217,2	K562	blood:
30	chr5:115418542..115422487-chr5:115423504..115427625,5	MCF-7	breast:
31	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
32	chr5:115445954..115448911-chr5:115452951..115455275,2	K562	blood:
33	chr5:115339171..115341772-chr5:115344562..115347685,3	K562	blood:
34	chr20:47537809..47538621-chr5:115628215..115629028,2	MCF-7	breast:
35	chr5:115512590..115515778-chr5:115516651..115520258,3	MCF-7	breast:
36	chr16:68772311..68772969-chr5:115376254..115377111,2	MCF-7	breast:
37	chr5:115402497..115406004-chr5:115407456..115411248,3	K562	blood:
38	chr5:115325463..115327847-chr5:115335444..115338217,2	K562	blood:
39	chr5:115418542..115422487-chr5:115423504..115427625,5	MCF-7	breast:
40	chr5:115412238..115416929-chr5:115418524..115421820,7	MCF-7	breast:
41	chr5:115685651..115688638-chr5:115690874..115693480,2	K562	blood:
42	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
43	chr16:3073983..3074533-chr5:115420524..115421124,2	Hela-S3	cervix:
44	chr5:115379424..115381506-chr5:115383490..115386090,2	K562	blood:
45	chr5:115176313..115177935-chr5:115421458..115423669,2	MCF-7	breast:
46	chr5:115374690..115378372-chr5:115418496..115424884,6	K562	blood:
47	chr5:115692236..115694986-chr5:115697167..115699493,2	MCF-7	breast:
48	chr17:39845051..39845605-chr5:115420384..115421275,2	Hela-S3	cervix:
49	chr5:115523919..115526832-chr5:115553749..115555427,2	MCF-7	breast:
50	chr5:114970091..114970643-chr5:115403493..115404412,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA6A-1	chr5:115710179-115710267	ENSG00000249280
2	lnc-SEMA6A-7	chr5:115553723-115553992	NONHSAT103356
3	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103358
4	lnc-LVRN.1-4	chr5:115637354-115638100	NONHSAT103359
5	lnc-LVRN.1-3	chr5:115549572-115550152	NONHSAT103355
6	lnc-LVRN.1-4	chr5:115638966-115639380	NONHSAT103359
7	lnc-COMMD10-8	chr5:115361675-115363300	NONHSAT103346
8	lnc-SEMA6A-1	chr5:115710179-115710267	NONHSAT103361
9	lnc-ATG12-5	chr5:115419504-115421113	ENSG00000271918.1
10	lnc-LVRN.1-4	chr5:115643332-115643482	NONHSAT103359
11	lnc-SEMA6A-1	chr5:115703287-115706170	ENSG00000249280
12	lnc-LVRN.1-4	chr5:115632111-115632653	NONHSAT103359
13	lnc-ATG12-5	chr5:115419214-115420722	NONHSAT103353
14	lnc-LVRN.1-4	chr5:115639227-115639380	NONHSAT103358
15	lnc-LVRN.1-4	chr5:115628154-115628257	NONHSAT103358
16	lnc-COMMD10-7	chr5:115365620-115367298	NONHSAT103348
17	lnc-COMMD10-6	chr5:115661716-115661988	l_3000_chr5:115661715-115668338_thyroid
18	lnc-SEMA6A-1	chr5:115708676-115708786	NONHSAT103361
19	lnc-COMMD10-6	chr5:115667126-115667860	l_3000_chr5:115661715-115668338_thyroid
20	lnc-COMMD10-8	chr5:115356724-115357449	NONHSAT103346
21	lnc-LVRN.1-4	chr5:115717975-115718151	NONHSAT103358
22	lnc-SEMA6A-1	chr5:115708676-115708786	ENSG00000249280
23	lnc-COMMD10-7	chr5:115367304-115367620	NONHSAT103348
24	lnc-SEMA6A-1	chr5:115703113-115706170	NONHSAT103361
25	lnc-COMMD10-6	chr5:115667915-115668338	l_3000_chr5:115661715-115668338_thyroid
26	lnc-COMMD10-8	chr5:115358088-115358163	NONHSAT103346
27	lnc-ATG12-4	chr5:115413807-115414267	ENSG00000272265.1
28	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103359
29	lnc-LVRN.1-4	chr5:115641553-115642622	NONHSAT103359

No data

Variant related genes	Relation type
ENSG00000185641	TF binding region
ENSG00000172901	TF binding region
ENSG00000271918	TF binding region
ARL14EPL	TF binding region
HMGN2P27	TF binding region
ENSG00000221778	TF binding region
COMMD10	TF binding region
ENSG00000272265	TF binding region
ENSG00000250015	TF binding region
RNU6-644P	TF binding region
ENSG00000268714	TF binding region
ENSG00000220996	TF binding region
ENSG00000248295	TF binding region
ENSG00000185641	CpG island
ENSG00000172901	CpG island
ENSG00000271918	CpG island
ARL14EPL	CpG island
HMGN2P27	CpG island
ENSG00000221778	CpG island
COMMD10	CpG island
ENSG00000272265	CpG island
ENSG00000250015	CpG island
RNU6-644P	CpG island
ENSG00000268714	CpG island
ENSG00000220996	CpG island
ENSG00000248295	CpG island
ENSG00000124198	chromatin interactions
ENSG00000131508	chromatin interactions
ENSG00000251201	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000212457	chromatin interactions
ENSG00000271931	chromatin interactions
ENSG00000146278	chromatin interactions
ENSG00000145781	chromatin interactions
ENSG00000221778	chromatin interactions
ENSG00000134970	chromatin interactions
ENSG00000243414	chromatin interactions
ENSG00000272265	chromatin interactions
ENSG00000268714	chromatin interactions
ENSG00000271918	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000172901	chromatin interactions
ENSG00000232916	chromatin interactions
ENSG00000232648	chromatin interactions
ENSG00000103145	chromatin interactions
ENSG00000131652	chromatin interactions
ENSG00000177879	chromatin interactions
ENSG00000248295	chromatin interactions
USP15	miRNA target sites
ACACA	miRNA target sites
BBC3	miRNA target sites

Extended variants
information (count: 20107 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:20107 , 50 per page) page: 1 2 3 4 5 6 7 ... 403

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17164372	chr5:115315944-115315945	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142150045	chr5:115315967-115315968	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs35582042	chr5:115315969-115315970	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs549536740	chr5:115315975-115315976	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs549848030	chr5:115316015-115316016	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs141288145	chr5:115316048-115316049	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs538482446	chr5:115316055-115316056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs558992885	chr5:115316064-115316065	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs373133098	chr5:115316073-115316074	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs143749160	chr5:115316074-115316075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs377266046	chr5:115316091-115316092	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs554498661	chr5:115316221-115316222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574504953	chr5:115316240-115316241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544086907	chr5:115316246-115316247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183043110	chr5:115316279-115316280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187378500	chr5:115316330-115316331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146784917	chr5:115316338-115316339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192110645	chr5:115316339-115316340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185090778	chr5:115316354-115316355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs377276023	chr5:115316355-115316356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190549333	chr5:115316361-115316362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560856875	chr5:115316371-115316372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140426363	chr5:115316391-115316392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574183274	chr5:115316392-115316393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150403823	chr5:115316452-115316453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192452126	chr5:115316490-115316491	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs138313417	chr5:115316510-115316511	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs149222702	chr5:115316581-115316582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17138520	chr5:115316588-115316589	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184302581	chr5:115316591-115316592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113572223	chr5:115316592-115316593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568112207	chr5:115316654-115316655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189675134	chr5:115316695-115316696	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs58088669	chr5:115316749-115316750	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs181041020	chr5:115316783-115316784	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs557619422	chr5:115316831-115316832	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs577432529	chr5:115316988-115316989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546477901	chr5:115317000-115317001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553563069	chr5:115317047-115317048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10478267	chr5:115317071-115317072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs184371089	chr5:115317075-115317076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143333716	chr5:115317076-115317077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529673946	chr5:115317077-115317078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543014749	chr5:115317128-115317129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563316420	chr5:115317137-115317138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532261210	chr5:115317162-115317163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189095437	chr5:115317183-115317184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372972711	chr5:115317186-115317187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377147243	chr5:115317225-115317226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73259384	chr5:115317250-115317251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Depressive disorder	21152026	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:4439 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115312200-115317200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:115313000-115316200	Enhancers	Adipose Nuclei	Adipose
3	chr5:115313000-115316200	Enhancers	NHDF-Ad	bronchial
4	chr5:115313000-115316800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:115313200-115316000	Enhancers	Osteobl	bone
6	chr5:115313200-115316400	Enhancers	Ovary	ovary
7	chr5:115313800-115316200	Enhancers	NHLF	lung
8	chr5:115313800-115317200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:115314000-115316200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:115314200-115316600	Enhancers	GM12878-XiMat	blood
11	chr5:115314600-115316200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:115314600-115316400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:115314800-115317000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr5:115315200-115316400	Weak transcription	HUVEC	blood vessel
15	chr5:115315200-115321800	Weak transcription	Fetal Muscle Leg	muscle
16	chr5:115315600-115316000	Enhancers	Rectal Smooth Muscle	rectum
17	chr5:115315800-115316000	Enhancers	Colon Smooth Muscle	Colon
18	chr5:115315800-115319400	Weak transcription	Fetal Lung	lung
19	chr5:115316000-115316800	Weak transcription	Osteobl	bone
20	chr5:115316200-115316800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:115316200-115320200	Weak transcription	Adipose Nuclei	Adipose
22	chr5:115316400-115316800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:115316400-115316800	Enhancers	HUVEC	blood vessel
24	chr5:115316400-115317600	Weak transcription	Ovary	ovary
25	chr5:115316800-115317000	Enhancers	Osteobl	bone
26	chr5:115316800-115320200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:115316800-115321600	Weak transcription	HUVEC	blood vessel
28	chr5:115317000-115321400	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr5:115317200-115317600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:115317200-115321800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:115317600-115318000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr5:115317600-115318200	Enhancers	Ovary	ovary
33	chr5:115318200-115319200	Weak transcription	Ovary	ovary
34	chr5:115319200-115319800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:115319200-115320000	Enhancers	Ovary	ovary
36	chr5:115319400-115323400	Enhancers	Fetal Lung	lung
37	chr5:115320000-115320800	Weak transcription	Ovary	ovary
38	chr5:115320200-115320800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:115320200-115322200	Strong transcription	Adipose Nuclei	Adipose
40	chr5:115320400-115320600	Weak transcription	Pancreas	Pancrea
41	chr5:115320600-115320800	Enhancers	Pancreas	Pancrea
42	chr5:115320800-115321800	Enhancers	Aorta	Aorta
43	chr5:115320800-115322000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:115320800-115322400	Enhancers	Ovary	ovary
45	chr5:115320800-115323800	Weak transcription	Pancreas	Pancrea
46	chr5:115321400-115324000	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr5:115321600-115322200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:115321600-115322400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr5:115321600-115322600	Enhancers	Fetal Heart	heart
50	chr5:115321600-115323800	Enhancers	HUVEC	blood vessel

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