Variant report

Variant	esv1811183
Chromosome Location	chr11:18389643-18432437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2314)
CpG islands
(count:1528)
Chromatin interactive
region (count:107)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:4)

(count:2314 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18417482-18418007	K562	blood:	n/a	n/a
2	ARID3A	chr11:18417363-18418020	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:18416098-18416266	K562	blood:	n/a	n/a
4	ARID3A	chr11:18415573-18416321	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:18405640-18406268	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:18405509-18405570	K562	blood:	n/a	n/a
7	ARID3A	chr11:18427130-18427330	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:18429056-18429644	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:18392884-18393113	K562	blood:	n/a	n/a
10	ATF1	chr11:18415850-18416263	K562	blood:	n/a	chr11:18416055-18416069
11	ATF1	chr11:18392904-18393138	K562	blood:	n/a	n/a
12	ATF2	chr11:18417358-18418006	GM12878	blood:	n/a	n/a
13	ATF2	chr11:18405250-18406175	GM12878	blood:	n/a	n/a
14	ATF2	chr11:18415770-18416297	H1-hESC	embryonic stem cell:	n/a	chr11:18416057-18416068 chr11:18416055-18416069
15	ATF2	chr11:18405190-18406276	GM12878	blood:	n/a	n/a
16	ATF2	chr11:18415680-18416405	GM12878	blood:	n/a	chr11:18416057-18416068 chr11:18416055-18416069
17	ATF2	chr11:18415816-18416330	GM12878	blood:	n/a	chr11:18416057-18416068 chr11:18416055-18416069
18	ATF2	chr11:18417310-18417823	GM12878	blood:	n/a	n/a
19	ATF3	chr11:18415639-18416275	K562	blood:	n/a	chr11:18416059-18416069 chr11:18416057-18416068 chr11:18416056-18416066 chr11:18416047-18416067 chr11:18416057-18416070 chr11:18416056-18416069 chr11:18416055-18416070 chr11:18416055-18416068 chr11:18416059-18416066 chr11:18416056-18416067 chr11:18416057-18416068 chr11:18416056-18416069 chr11:18416056-18416066
20	ATF3	chr11:18415784-18416272	K562	blood:	n/a	chr11:18416059-18416069 chr11:18416057-18416068 chr11:18416056-18416066 chr11:18416047-18416067 chr11:18416057-18416070 chr11:18416056-18416069 chr11:18416055-18416070 chr11:18416055-18416068 chr11:18416059-18416066 chr11:18416056-18416067 chr11:18416057-18416068 chr11:18416056-18416069 chr11:18416056-18416066
21	ATF3	chr11:18415702-18416393	A549	lung:	n/a	chr11:18416059-18416069 chr11:18416057-18416068 chr11:18416056-18416066 chr11:18416047-18416067 chr11:18416057-18416070 chr11:18416056-18416069 chr11:18416055-18416070 chr11:18416055-18416068 chr11:18416059-18416066 chr11:18416056-18416067 chr11:18416057-18416068 chr11:18416056-18416069 chr11:18416056-18416066
22	ATF3	chr11:18405049-18406253	A549	lung:	n/a	n/a
23	ATF3	chr11:18404979-18405669	A549	lung:	n/a	n/a
24	BACH1	chr11:18405354-18405361	K562	blood:	n/a	n/a
25	BACH1	chr11:18416069-18416320	K562	blood:	n/a	n/a
26	BACH1	chr11:18411732-18411980	K562	blood:	n/a	chr11:18411800-18411814
27	BACH1	chr11:18415784-18416220	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr11:18417513-18418052	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr11:18414386-18414632	GM12878	blood:	n/a	chr11:18414481-18414492
30	BATF	chr11:18405254-18405807	GM12878	blood:	n/a	n/a
31	BCL3	chr11:18415390-18416521	A549	lung:	n/a	n/a
32	BCL3	chr11:18415762-18416331	GM12878	blood:	n/a	n/a
33	BCL3	chr11:18429501-18430863	K562	blood:	n/a	n/a
34	BCL3	chr11:18430222-18430427	K562	blood:	n/a	n/a
35	BCL3	chr11:18417130-18418132	A549	lung:	n/a	n/a
36	BCL3	chr11:18415357-18416142	A549	lung:	n/a	n/a
37	BCL3	chr11:18428976-18431218	A549	lung:	n/a	n/a
38	BCL3	chr11:18405074-18406342	A549	lung:	n/a	chr11:18405880-18405888
39	BCL3	chr11:18430078-18430741	GM12878	blood:	n/a	n/a
40	BCL3	chr11:18417090-18418017	A549	lung:	n/a	n/a
41	BCL3	chr11:18404658-18406453	A549	lung:	n/a	chr11:18405880-18405888 chr11:18405033-18405042
42	BCL3	chr11:18429952-18430937	A549	lung:	n/a	n/a
43	BCLAF1	chr11:18430346-18430780	GM12878	blood:	n/a	n/a
44	BCLAF1	chr11:18415360-18416445	GM12878	blood:	n/a	n/a
45	BCLAF1	chr11:18430160-18430545	K562	blood:	n/a	n/a
46	BCLAF1	chr11:18405255-18405911	GM12878	blood:	n/a	chr11:18405880-18405888
47	BCLAF1	chr11:18405092-18405956	GM12878	blood:	n/a	chr11:18405880-18405888
48	BCLAF1	chr11:18417265-18418037	K562	blood:	n/a	n/a
49	BHLHE40	chr11:18405300-18406209	GM12878	blood:	n/a	n/a
50	BHLHE40	chr11:18405048-18405124	K562	blood:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18415641-18415691	AG10803	skin:	n/a
2	chr11:18415711-18415761	HIPEpiC	eye:	n/a
3	chr11:18429080-18429130	HUVEC	blood vessel:	n/a
4	chr11:18415641-18415691	AG10803	skin:	n/a
5	chr11:18415711-18415761	HIPEpiC	eye:	n/a
6	chr11:18429080-18429130	HUVEC	blood vessel:	n/a
7	chr11:18415880-18415930	PrEC	prostate:	n/a
8	chr11:18417757-18417807	CMK	blood:	n/a
9	chr11:18415850-18415900	PFSK-1	brain:	n/a
10	chr11:18414888-18414938	HMEC	breast:	n/a
11	chr11:18415989-18416039	U87	brain:	n/a
12	chr11:18415964-18416014	GM06990	blood:	n/a
13	chr11:18415850-18415900	AG10803	skin:	n/a
14	chr11:18417779-18417829	BE2_C	brain:	n/a
15	chr11:18417757-18417807	HL-60	blood:	n/a
16	chr11:18416547-18416597	ECC-1	luminal epithelium:	n/a
17	chr11:18417832-18417882	HUVEC	blood vessel:	n/a
18	chr11:18417779-18417829	Hepatocyte	liver:	n/a
19	chr11:18416767-18416817	Jurkat	blood:	n/a
20	chr11:18415989-18416039	ProgFib	skin:	n/a
21	chr11:18417840-18417890	HepG2	liver:	n/a
22	chr11:18429080-18429130	HIPEpiC	eye:	n/a
23	chr11:18416535-18416585	MCF10A-Er-Src	breast:	n/a
24	chr11:18415927-18415977	GM12891	blood:	n/a
25	chr11:18417840-18417890	HAEpiC	amniotic membrane:	n/a
26	chr11:18415927-18415977	HepG2	liver:	n/a
27	chr11:18417924-18417974	CMK	blood:	n/a
28	chr11:18415874-18415924	BE2_C	brain:	n/a
29	chr11:18416224-18416274	HNPCEpiC	eye:	n/a
30	chr11:18419598-18419648	SK-N-SH	brain:	n/a
31	chr11:18415874-18415924	AG10803	skin:	n/a
32	chr11:18414888-18414938	HCM	heart:	n/a
33	chr11:18415880-18415930	IMR90	lung:	fetal
34	chr11:18417924-18417974	MCF10A-Er-Src	breast:	n/a
35	chr11:18415989-18416039	Jurkat	blood:	n/a
36	chr11:18419598-18419648	HNPCEpiC	eye:	n/a
37	chr11:18416224-18416274	AG04449	skin:	fetal
38	chr11:18415711-18415761	AG10803	skin:	n/a
39	chr11:18419598-18419648	AG04449	skin:	fetal
40	chr11:18417840-18417890	LNCaP	prostate:	n/a
41	chr11:18417767-18417817	GM12878	blood:	n/a
42	chr11:18415850-18415900	U87	brain:	n/a
43	chr11:18415874-18415924	CMK	blood:	n/a
44	chr11:18416767-18416817	HIPEpiC	eye:	n/a
45	chr11:18416535-18416585	HEK293	kidney:	embryo
46	chr11:18414888-18414938	HCF	heart:	n/a
47	chr11:18415711-18415761	HepG2	liver:	n/a
48	chr11:18412294-18412344	AG09319	gingival:	n/a
49	chr11:18417924-18417974	SKMC	muscle:	n/a
50	chr11:18417779-18417829	PFSK-1	brain:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:11968050..11968943-chr11:18415825..18416455,2	Hela-S3	cervix:
2	chr1:117908068..117910617-chr11:18415187..18418094,2	MCF-7	breast:
3	chr11:18417328..18418003-chr2:32581821..32582442,2	Hela-S3	cervix:
4	chr11:18430626..18432747-chr11:18545645..18547445,2	K562	blood:
5	chr11:18339570..18341563-chr11:18389035..18391001,2	K562	blood:
6	chr11:18417529..18418347-chr16:14726603..14727124,2	Hela-S3	cervix:
7	chr11:18404260..18406442-chr11:18407385..18409678,2	MCF-7	breast:
8	chr11:18343277..18345280-chr11:18409232..18413616,5	MCF-7	breast:
9	chr11:18415665..18418550-chr11:18429109..18431220,2	MCF-7	breast:
10	chr11:18400049..18401686-chr11:18404314..18405882,2	K562	blood:
11	chr11:18415715..18416570-chr12:64845567..64846239,2	Hela-S3	cervix:
12	chr11:18402803..18405154-chr11:18406672..18408656,2	K562	blood:
13	chr11:18416119..18416955-chr7:99933156..99933912,2	Hela-S3	cervix:
14	chr11:18342491..18345045-chr11:18415566..18419495,5	MCF-7	breast:
15	chr11:18415664..18416440-chr18:71815010..71815580,2	Hela-S3	cervix:
16	chr11:18415553..18416068-chr5:175815719..175816243,2	Hela-S3	cervix:
17	chr11:18417817..18418493-chr3:73160074..73160630,2	Hela-S3	cervix:
18	chr11:18429496..18431588-chr11:18458511..18461417,2	K562	blood:
19	chr11:18389829..18393207-chr11:18415267..18417660,3	K562	blood:
20	chr11:18415810..18416651-chr8:67579307..67579955,2	Hela-S3	cervix:
21	chr11:18401037..18403856-chr11:18413417..18417997,5	K562	blood:
22	chr11:18342186..18344992-chr11:18392996..18395179,2	K562	blood:
23	chr11:18416054..18417892-chr11:18432317..18434579,2	K562	blood:
24	chr11:18417413..18418232-chr6:74230151..74230823,2	Hela-S3	cervix:
25	chr11:18414795..18417618-chr11:18546727..18549809,4	MCF-7	breast:
26	chr11:18400049..18401686-chr11:18404314..18405882,2	K562	blood:
27	chr11:18406695..18409198-chr11:18428247..18430111,2	K562	blood:
28	chr11:18342292..18344024-chr11:18424254..18426618,2	MCF-7	breast:
29	chr11:18415801..18416462-chr12:92539739..92540347,2	Hela-S3	cervix:
30	chr11:18416876..18417614-chr3:115771645..115772165,2	Hela-S3	cervix:
31	chr11:18342812..18343809-chr11:18416058..18416846,3	NB4	blood:
32	chr11:18401460..18405154-chr11:18406672..18408749,3	K562	blood:
33	chr11:18429142..18431296-chr11:18432609..18435165,2	K562	blood:
34	chr11:18414619..18417567-chr11:18475840..18478644,2	K562	blood:
35	chr11:18414611..18420404-chr11:18425224..18433817,11	K562	blood:
36	chr11:18428578..18433796-chr11:18433952..18441799,12	K562	blood:
37	chr11:18398568..18400836-chr11:18427462..18430326,2	MCF-7	breast:
38	chr11:18404604..18407545-chr11:18408793..18411812,5	K562	blood:
39	chr11:18430457..18432481-chr11:18456231..18458824,2	K562	blood:
40	chr11:18386073..18387800-chr11:18389640..18392386,2	K562	blood:
41	chr11:18365375..18369096-chr11:18414733..18417585,5	MCF-7	breast:
42	chr11:18405238..18405993-chr9:33817340..33817887,2	Hela-S3	cervix:
43	chr11:18390732..18392479-chr11:18415393..18418299,2	MCF-7	breast:
44	chr11:18416054..18417892-chr11:18432317..18434579,2	K562	blood:
45	chr11:18338559..18340815-chr11:18429973..18431538,2	K562	blood:
46	chr11:18415873..18420206-chr11:18430045..18435036,6	MCF-7	breast:
47	chr11:18415399..18418482-chr11:18547632..18550708,3	MCF-7	breast:
48	chr11:18417263..18417821-chr12:51441625..51442366,2	Hela-S3	cervix:
49	chr11:18415166..18418061-chr11:18653248..18658001,5	K562	blood:
50	chr11:18349981..18351945-chr11:18404895..18407239,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LDHC-1	chr11:18428199-18428278	ENSG00000256006.1
2	lnc-GTF2H1-2	chr11:18397373-18397741	NONHSAT018282
3	lnc-LDHC-2	chr11:18416108-18416183	NONHSAT018284
4	lnc-GTF2H1-1	chr11:18394180-18394431	NONHSAT018281
5	lnc-LDHC-1	chr11:18427156-18427345	ENSG00000256006.1
6	lnc-LDHC-2	chr11:18418366-18418945	NONHSAT018284

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3159	chr11:18409343-18409364	MIMAT0015033

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	LDHA	hsa-miR-34a-5p	chr11:18429085-18429092
2	LDHA	hsa-miR-33a-5p	chr11:18429322-18429340
3	LDHA	hsa-miR-33a-5p	chr11:18429333-18429340
4	LDHA	hsa-miR-34a-5p	chr11:18429069-18429092

Variant related genes	Relation type
ENSG00000256006	TF binding region
LDHC	TF binding region
LDHA	TF binding region
MIR3159	TF binding region
ENSG00000256006	CpG island
LDHC	CpG island
LDHA	CpG island
MIR3159	CpG island
ENSG00000134333	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000188486	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000133112	chromatin interactions
ENSG00000198162	chromatin interactions
ENSG00000264920	chromatin interactions
ENSG00000271427	chromatin interactions
ENSG00000141665	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000074319	chromatin interactions
ENSG00000110696	chromatin interactions
ENSG00000167182	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000242294	chromatin interactions
ENSG00000166796	chromatin interactions
ENSG00000256006	chromatin interactions
ENSG00000179826	chromatin interactions
ENSG00000183735	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000183431	chromatin interactions
ENSG00000213865	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000175073	chromatin interactions
ENSG00000111676	chromatin interactions
ENSG00000151116	chromatin interactions
ENSG00000270024	chromatin interactions
ENSG00000121716	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000177225	chromatin interactions
ENSG00000107341	chromatin interactions
ENSG00000198408	chromatin interactions
ENSG00000115760	chromatin interactions
ENSG00000139726	chromatin interactions
ENSG00000125534	chromatin interactions
ENSG00000110756	chromatin interactions
ENSG00000264603	chromatin interactions
ENSG00000166800	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000100612	chromatin interactions
ENSG00000172590	chromatin interactions
ENSG00000197362	chromatin interactions
ENSG00000048162	chromatin interactions
ENSG00000103429	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000110768	chromatin interactions
ENSG00000170919	chromatin interactions
ENSG00000255284	chromatin interactions
ENSG00000050426	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000272752	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000179119	chromatin interactions
ENSG00000146066	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000140299	chromatin interactions

Extended variants
information (count: 1948 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1948 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553857733	chr11:18389667-18389668	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553139918	chr11:18389736-18389737	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574306546	chr11:18389752-18389753	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112710585	chr11:18389775-18389776	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572544684	chr11:18389800-18389801	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192547061	chr11:18389820-18389821	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577948639	chr11:18389875-18389876	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562653206	chr11:18389877-18389878	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557962764	chr11:18389903-18389904	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538621437	chr11:18389947-18389948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576142871	chr11:18389966-18389967	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184514508	chr11:18389974-18389975	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73434649	chr11:18389988-18389989	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575760446	chr11:18390048-18390049	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs74610672	chr11:18390067-18390068	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543251322	chr11:18390078-18390079	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189038320	chr11:18390097-18390098	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115290251	chr11:18390204-18390205	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78197521	chr11:18390240-18390241	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181990360	chr11:18390271-18390272	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551173078	chr11:18390302-18390303	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184833016	chr11:18390436-18390437	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs564718664	chr11:18390445-18390446	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531760570	chr11:18390472-18390473	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4757642	chr11:18390489-18390490	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs189201826	chr11:18390526-18390527	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs58330608	chr11:18390560-18390561	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145707015	chr11:18390588-18390589	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375130129	chr11:18390611-18390612	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79474472	chr11:18390632-18390633	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372788508	chr11:18390667-18390668	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375917797	chr11:18390691-18390692	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141855969	chr11:18390701-18390702	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539958441	chr11:18390704-18390705	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557939549	chr11:18390722-18390723	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532961542	chr11:18390785-18390786	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369791414	chr11:18390791-18390792	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79672940	chr11:18390843-18390844	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537200086	chr11:18390844-18390845	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555589617	chr11:18390873-18390874	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528163005	chr11:18390930-18390931	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181558658	chr11:18390933-18390934	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186525356	chr11:18390944-18390945	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538266328	chr11:18390987-18390988	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552967111	chr11:18391090-18391091	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577529775	chr11:18391116-18391117	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544653776	chr11:18391197-18391198	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs545109448	chr11:18391214-18391215	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10832923	chr11:18391237-18391238	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs531798119	chr11:18391248-18391249	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1730 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18345000-18405000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:18346800-18390400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:18361800-18391600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:18363000-18390200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:18363200-18393000	Weak transcription	Fetal Heart	heart
6	chr11:18367600-18390000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:18373200-18390600	Strong transcription	Adipose Nuclei	Adipose
8	chr11:18373400-18390000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:18373400-18390400	Strong transcription	Dnd41	blood
10	chr11:18373600-18389800	Strong transcription	Liver	Liver
11	chr11:18373600-18389800	Strong transcription	Duodenum Mucosa	Duodenum
12	chr11:18373600-18390200	Strong transcription	Fetal Thymus	thymus
13	chr11:18373600-18390400	Strong transcription	Placenta	Placenta
14	chr11:18373600-18391200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr11:18373800-18390400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:18374800-18389800	Strong transcription	Fetal Muscle Leg	muscle
17	chr11:18374800-18390200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:18377200-18390000	Strong transcription	Fetal Brain Female	brain
19	chr11:18382600-18390400	Strong transcription	Primary B cells from cord blood	blood
20	chr11:18382800-18390000	Strong transcription	Brain Cingulate Gyrus	brain
21	chr11:18383800-18390000	Weak transcription	Fetal Brain Male	brain
22	chr11:18383800-18390000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr11:18383800-18391400	Weak transcription	Colonic Mucosa	Colon
24	chr11:18385000-18390000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr11:18385000-18392600	Weak transcription	Small Intestine	intestine
26	chr11:18385800-18389800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr11:18386000-18390400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr11:18386200-18389800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr11:18387000-18390000	Weak transcription	Right Atrium	heart
30	chr11:18387400-18390000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:18387600-18389800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr11:18387600-18390600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr11:18387600-18390600	Weak transcription	Spleen	Spleen
34	chr11:18387600-18391200	Weak transcription	Brain Angular Gyrus	brain
35	chr11:18387600-18391400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr11:18387600-18391400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:18387600-18391400	Weak transcription	Aorta	Aorta
38	chr11:18387600-18391400	Weak transcription	Right Ventricle	heart
39	chr11:18387600-18391600	Enhancers	Primary hematopoietic stem cells	blood
40	chr11:18387600-18393200	Weak transcription	Gastric	stomach
41	chr11:18387600-18394000	Weak transcription	Fetal Stomach	stomach
42	chr11:18387600-18395400	Weak transcription	Lung	lung
43	chr11:18387600-18398600	Weak transcription	Ovary	ovary
44	chr11:18387600-18404200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:18387600-18404400	Weak transcription	Esophagus	oesophagus
46	chr11:18387600-18404800	Weak transcription	Pancreas	Pancrea
47	chr11:18387800-18391000	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:18387800-18404400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr11:18388000-18389800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:18388000-18390000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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