Variant report

Variant	nsv1067252
Chromosome Location	chr18:29475073-29583744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:917)
Chromatin interactive
region (count:71)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29545658-29545826	K562	blood:	n/a	n/a
2	ARID3A	chr18:29532310-29532545	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29522908-29523247	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29557377-29557689	K562	blood:	n/a	n/a
5	ARID3A	chr18:29534309-29534712	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29523487-29524214	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29524025-29524906	K562	blood:	n/a	n/a
8	ARID3A	chr18:29557292-29557535	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:29523384-29523668	K562	blood:	n/a	n/a
10	ARID3A	chr18:29537022-29537114	K562	blood:	n/a	n/a
11	ATF1	chr18:29524097-29524682	K562	blood:	n/a	n/a
12	ATF2	chr18:29522789-29523752	GM12878	blood:	n/a	n/a
13	ATF2	chr18:29536816-29537133	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr18:29522071-29522586	GM12878	blood:	n/a	n/a
15	ATF2	chr18:29526686-29527108	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr18:29570743-29571182	GM12878	blood:	n/a	n/a
17	ATF2	chr18:29557219-29557644	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr18:29522911-29523275	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr18:29523281-29523810	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr18:29522854-29523220	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr18:29522919-29523241	H1-hESC	embryonic stem cell:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
22	ATF3	chr18:29522864-29523406	HepG2	liver:	n/a	chr18:29523114-29523123 chr18:29523103-29523123 chr18:29523311-29523319 chr18:29523239-29523248
23	ATF3	chr18:29522850-29523231	GM12878	blood:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
24	ATF3	chr18:29522931-29523228	K562	blood:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
25	ATF3	chr18:29522818-29523234	H1-hESC	embryonic stem cell:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
26	ATF3	chr18:29522915-29523195	HepG2	liver:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
27	ATF3	chr18:29523004-29523182	GM12878	blood:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
28	BACH1	chr18:29557475-29557490	K562	blood:	n/a	n/a
29	BACH1	chr18:29523016-29523134	K562	blood:	n/a	n/a
30	BACH1	chr18:29557332-29557688	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr18:29522805-29523692	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr18:29521754-29521776	K562	blood:	n/a	n/a
33	BCL11A	chr18:29570839-29571146	GM12878	blood:	n/a	n/a
34	BCL11A	chr18:29523250-29523543	GM12878	blood:	n/a	n/a
35	BCL11A	chr18:29570849-29571082	GM12878	blood:	n/a	n/a
36	BCLAF1	chr18:29523284-29523848	GM12878	blood:	n/a	n/a
37	BCLAF1	chr18:29522069-29523233	GM12878	blood:	n/a	chr18:29522744-29522753 chr18:29523208-29523217 chr18:29523170-29523179
38	BCLAF1	chr18:29522756-29523235	GM12878	blood:	n/a	chr18:29523208-29523217 chr18:29523170-29523179
39	BCLAF1	chr18:29523293-29523754	GM12878	blood:	n/a	n/a
40	BCLAF1	chr18:29570709-29571250	GM12878	blood:	n/a	n/a
41	BHLHE40	chr18:29534485-29534681	K562	blood:	n/a	n/a
42	BHLHE40	chr18:29536920-29537206	K562	blood:	n/a	n/a
43	BHLHE40	chr18:29534377-29534734	HepG2	liver:	n/a	n/a
44	BHLHE40	chr18:29536921-29537061	GM12878	blood:	n/a	n/a
45	BHLHE40	chr18:29557383-29557574	K562	blood:	n/a	n/a
46	BHLHE40	chr18:29522137-29523985	HepG2	liver:	n/a	chr18:29523112-29523125 chr18:29523114-29523123 chr18:29523115-29523124 chr18:29523108-29523129 chr18:29523114-29523123 chr18:29522742-29522758
47	BHLHE40	chr18:29522115-29523849	K562	blood:	n/a	chr18:29523112-29523125 chr18:29523114-29523123 chr18:29523115-29523124 chr18:29523108-29523129 chr18:29523114-29523123 chr18:29522742-29522758
48	BHLHE40	chr18:29536923-29537211	HepG2	liver:	n/a	n/a
49	BHLHE40	chr18:29522205-29523879	GM12878	blood:	n/a	chr18:29523112-29523125 chr18:29523114-29523123 chr18:29523115-29523124 chr18:29523108-29523129 chr18:29523114-29523123 chr18:29522742-29522758
50	BHLHE40	chr18:29522943-29523252	A549	lung:	n/a	chr18:29523112-29523125 chr18:29523114-29523123 chr18:29523115-29523124 chr18:29523108-29523129 chr18:29523114-29523123

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29522728-29522778	GM12878	blood:	n/a
2	chr18:29522728-29522778	PANC-1	pancreas:	n/a
3	chr18:29522728-29522778	GM12878	blood:	n/a
4	chr18:29522728-29522778	PANC-1	pancreas:	n/a
5	chr18:29523289-29523339	ECC-1	luminal epithelium:	n/a
6	chr18:29522434-29522484	K562	blood:	n/a
7	chr18:29523271-29523321	HCPEpiC	choroid plexus:	n/a
8	chr18:29519807-29519857	Hela-S3	cervix:	n/a
9	chr18:29523277-29523327	HPAEpiC	pulmonary alveolar:	n/a
10	chr18:29523380-29523430	HCPEpiC	choroid plexus:	n/a
11	chr18:29522728-29522778	T-47D	breast:	n/a
12	chr18:29523277-29523327	HCF	heart:	n/a
13	chr18:29522262-29522312	HAEpiC	amniotic membrane:	n/a
14	chr18:29523426-29523476	HEK293	kidney:	embryo
15	chr18:29519807-29519857	HPAEpiC	pulmonary alveolar:	n/a
16	chr18:29522728-29522778	NT2-D1	testis:	n/a
17	chr18:29523380-29523430	HCF	heart:	n/a
18	chr18:29523289-29523339	BJ	skin:	n/a
19	chr18:29523380-29523430	HEK293	kidney:	embryo
20	chr18:29522728-29522778	PrEC	prostate:	n/a
21	chr18:29522434-29522484	GM12891	blood:	n/a
22	chr18:29522434-29522484	HepG2	liver:	n/a
23	chr18:29523271-29523321	HCM	heart:	n/a
24	chr18:29523426-29523476	NT2-D1	testis:	n/a
25	chr18:29523078-29523128	A549	lung:	n/a
26	chr18:29523426-29523476	AoSMC	blood vessel:	n/a
27	chr18:29522262-29522312	AG09309	skin:	n/a
28	chr18:29519807-29519857	NHBE	bronchial:	n/a
29	chr18:29525892-29525942	AG04450	lung:	fetal
30	chr18:29523728-29523778	HMEC	breast:	n/a
31	chr18:29523271-29523321	Caco-2	colon:	n/a
32	chr18:29523426-29523476	HMEC	breast:	n/a
33	chr18:29523426-29523476	HNPCEpiC	eye:	n/a
34	chr18:29525892-29525942	AG09319	gingival:	n/a
35	chr18:29522957-29523007	SK-N-SH	brain:	n/a
36	chr18:29523277-29523327	AG04449	skin:	fetal
37	chr18:29519807-29519857	Caco-2	colon:	n/a
38	chr18:29523078-29523128	CMK	blood:	n/a
39	chr18:29523063-29523113	NHBE	bronchial:	n/a
40	chr18:29523063-29523113	CMK	blood:	n/a
41	chr18:29522262-29522312	K562	blood:	n/a
42	chr18:29523728-29523778	HEEpiC	esophagus:	n/a
43	chr18:29525892-29525942	HUVEC	blood vessel:	n/a
44	chr18:29523728-29523778	H1-hESC	embryonic stem cell:	embryo
45	chr18:29523380-29523430	K562	blood:	n/a
46	chr18:29523289-29523339	HNPCEpiC	eye:	n/a
47	chr18:29523277-29523327	Hepatocyte	liver:	n/a
48	chr18:29523277-29523327	AG10803	skin:	n/a
49	chr18:29523063-29523113	HepG2	liver:	n/a
50	chr18:29522957-29523007	RPTEC	kidney:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:29469874..29472927-chr18:29473896..29477156,4	K562	blood:
2	chr18:29523882..29525586-chr18:29646566..29649385,2	K562	blood:
3	chr18:29474340..29476672-chr18:29479905..29482693,2	K562	blood:
4	chr18:29522626..29525135-chr18:29528415..29529942,2	K562	blood:
5	chr18:29517111..29520943-chr18:29521139..29523956,5	MCF-7	breast:
6	chr18:29473750..29476339-chr18:29521274..29523147,2	K562	blood:
7	chr18:29490577..29492633-chr18:29522032..29523871,2	MCF-7	breast:
8	chr18:29503480..29505119-chr18:29513383..29515079,2	K562	blood:
9	chr18:29503360..29505001-chr18:29640249..29641750,2	K562	blood:
10	chr18:29509835..29512655-chr18:29521511..29523719,2	MCF-7	breast:
11	chr18:29518719..29521005-chr18:29521192..29525426,5	MCF-7	breast:
12	chr18:29499375..29501591-chr18:29520871..29523624,3	K562	blood:
13	chr18:29485958..29488048-chr18:29520164..29521790,2	K562	blood:
14	chr18:29513029..29515925-chr18:29517093..29518613,2	K562	blood:
15	chr18:29494660..29496304-chr18:29519916..29522258,2	K562	blood:
16	chr18:29475912..29478004-chr18:29521825..29524429,2	MCF-7	breast:
17	chr18:29493108..29495287-chr18:29497330..29499746,2	K562	blood:
18	chr18:29487420..29490004-chr18:29496191..29498820,2	K562	blood:
19	chr18:29503480..29506352-chr18:29513383..29515079,3	K562	blood:
20	chr18:29503297..29506681-chr18:29521643..29525244,4	K562	blood:
21	chr18:29570336..29572597-chr18:29669436..29671957,2	K562	blood:
22	chr18:29506087..29508444-chr18:29510343..29513453,3	MCF-7	breast:
23	chr18:29457834..29460225-chr18:29482969..29485185,2	MCF-7	breast:
24	chr18:29521939..29525237-chr18:29670716..29673913,4	MCF-7	breast:
25	chr18:29503480..29505119-chr18:29513383..29515079,2	K562	blood:
26	chr18:29531400..29532947-chr18:29534853..29537297,2	K562	blood:
27	chr18:29511145..29516088-chr18:29521483..29523975,5	MCF-7	breast:
28	chr18:29521537..29525393-chr18:29670839..29674328,7	K562	blood:
29	chr18:29521522..29523729-chr18:29672844..29674625,2	MCF-7	breast:
30	chr18:29520544..29523172-chr18:33708356..33710539,2	K562	blood:
31	chr18:29490421..29492288-chr18:29494638..29497276,2	K562	blood:
32	chr18:29501674..29503497-chr18:29522527..29524041,2	MCF-7	breast:
33	chr18:29523716..29526205-chr18:29536614..29539662,3	K562	blood:
34	chr18:29492718..29495244-chr18:29521543..29523372,2	MCF-7	breast:
35	chr18:29522234..29525588-chr18:29534457..29537204,4	MCF-7	breast:
36	chr18:29523716..29526205-chr18:29536614..29539662,3	K562	blood:
37	chr18:29521665..29524441-chr18:29544834..29547590,2	K562	blood:
38	chr18:29522249..29524505-chr18:29596603..29599089,2	MCF-7	breast:
39	chr18:29520857..29524705-chr18:29670705..29674434,7	K562	blood:
40	chr18:29522696..29523369-chr18:29598378..29599258,2	Hela-S3	cervix:
41	chr1:154155258..154156060-chr18:29522614..29523350,2	Hela-S3	cervix:
42	chr18:29477012..29478929-chr18:29485217..29488181,2	K562	blood:
43	chr18:29485958..29488048-chr18:29520164..29521790,2	K562	blood:
44	chr18:29494660..29496304-chr18:29519916..29522258,2	K562	blood:
45	chr18:29506087..29508444-chr18:29510343..29513453,3	MCF-7	breast:
46	chr18:29468408..29471507-chr18:29523062..29524905,3	K562	blood:
47	chr18:29490307..29491921-chr18:29494473..29497276,2	K562	blood:
48	chr18:29477012..29478929-chr18:29485217..29488181,2	K562	blood:
49	chr18:29490307..29491921-chr18:29494473..29497276,2	K562	blood:
50	chr18:29518719..29521005-chr18:29521192..29525426,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRAPPC8-3	chr18:29533013-29533099	NONHSAT058843
2	lnc-TRAPPC8-3	chr18:29519358-29519707	NONHSAT058843

No data

Variant related genes	Relation type
ENSG00000263823	TF binding region
PGDP1	TF binding region
TRAPPC8	TF binding region
RNU6-1050P	TF binding region
ENSG00000266105	TF binding region
ENSG00000263823	CpG island
PGDP1	CpG island
TRAPPC8	CpG island
RNU6-1050P	CpG island
ENSG00000266105	CpG island
ENSG00000134758	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000141424	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000134759	chromatin interactions
ENSG00000101695	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000263917	chromatin interactions
ENSG00000265063	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000153339	chromatin interactions
ENSG00000222320	chromatin interactions
ENSG00000266105	chromatin interactions
ENSG00000143641	chromatin interactions
ENSG00000238982	chromatin interactions
ENSG00000263823	chromatin interactions

Extended variants
information (count: 4485 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4485 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577139077	chr18:29475074-29475075	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs568584220	chr18:29475105-29475106	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531927036	chr18:29475106-29475107	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs199506785	chr18:29475114-29475115	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139118581	chr18:29475154-29475155	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs530085392	chr18:29475184-29475185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541850772	chr18:29475209-29475210	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560671479	chr18:29475214-29475215	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527762331	chr18:29475218-29475219	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs552371266	chr18:29475315-29475316	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373502403	chr18:29475326-29475327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183433307	chr18:29475444-29475445	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs187968933	chr18:29475465-29475466	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192825757	chr18:29475484-29475485	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568421926	chr18:29475488-29475489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183485242	chr18:29475500-29475501	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs565794389	chr18:29475506-29475507	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs547006942	chr18:29475522-29475523	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs539130980	chr18:29475537-29475538	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs142410259	chr18:29475569-29475570	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565323585	chr18:29475578-29475579	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576978376	chr18:29475645-29475646	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs187406738	chr18:29475646-29475647	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs556482898	chr18:29475688-29475689	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs34180462	chr18:29475691-29475692	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192593048	chr18:29475731-29475732	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529393197	chr18:29475778-29475779	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs7244508	chr18:29475779-29475780	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs572520020	chr18:29475818-29475819	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184817641	chr18:29475826-29475827	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs188412104	chr18:29475833-29475834	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146002928	chr18:29475997-29475998	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78260612	chr18:29476036-29476037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs77265120	chr18:29476037-29476038	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549991610	chr18:29476092-29476093	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537261666	chr18:29476101-29476102	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139901707	chr18:29476160-29476161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529151106	chr18:29476196-29476197	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs143508189	chr18:29476198-29476199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs555225387	chr18:29476238-29476239	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539526288	chr18:29476275-29476276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12955454	chr18:29476282-29476283	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs145656308	chr18:29476286-29476287	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs62095547	chr18:29476331-29476332	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544687720	chr18:29476339-29476340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs62095548	chr18:29476403-29476404	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs560505980	chr18:29476461-29476462	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs192268095	chr18:29476526-29476527	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185060871	chr18:29476544-29476545	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148478371	chr18:29476550-29476551	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1994 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29405600-29481800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:29406200-29518600	Weak transcription	Fetal Brain Male	brain
3	chr18:29417600-29515600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:29431800-29499000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr18:29431800-29512600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr18:29432400-29480000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr18:29432600-29481600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr18:29432600-29507600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr18:29432600-29521400	Weak transcription	Stomach Mucosa	stomach
10	chr18:29446000-29489000	Strong transcription	Fetal Thymus	thymus
11	chr18:29449200-29489000	Strong transcription	Adipose Nuclei	Adipose
12	chr18:29456000-29479200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr18:29456000-29480000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr18:29457000-29480400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr18:29457000-29505800	Weak transcription	Brain Angular Gyrus	brain
16	chr18:29457200-29479600	Weak transcription	Colonic Mucosa	Colon
17	chr18:29457200-29493200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr18:29457400-29479800	Weak transcription	Pancreas	Pancrea
19	chr18:29457400-29484800	Weak transcription	NHEK	skin
20	chr18:29457600-29479800	Weak transcription	Right Ventricle	heart
21	chr18:29458200-29479600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr18:29458200-29479600	Weak transcription	Aorta	Aorta
23	chr18:29458200-29479600	Weak transcription	Esophagus	oesophagus
24	chr18:29458200-29482600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr18:29458600-29485200	Weak transcription	Brain Substantia Nigra	brain
26	chr18:29459000-29481400	Weak transcription	NHLF	lung
27	chr18:29460400-29501200	Strong transcription	Liver	Liver
28	chr18:29461400-29494200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr18:29461600-29491200	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr18:29461600-29518600	Weak transcription	Psoas Muscle	Psoas
31	chr18:29462000-29520000	Weak transcription	Fetal Heart	heart
32	chr18:29462400-29476400	Strong transcription	Primary T cells from cord blood	blood
33	chr18:29462400-29476600	Weak transcription	HUVEC	blood vessel
34	chr18:29462600-29479800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr18:29462600-29485800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr18:29462600-29489000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr18:29462800-29485200	Weak transcription	Brain Germinal Matrix	brain
38	chr18:29462800-29486000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr18:29463200-29490200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr18:29463400-29509200	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr18:29463600-29481600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr18:29463800-29477800	Weak transcription	Colon Smooth Muscle	Colon
43	chr18:29464400-29479600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr18:29464600-29477800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr18:29465000-29489200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr18:29465600-29480200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr18:29466200-29486000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr18:29466200-29489000	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr18:29466400-29490800	Strong transcription	Placenta	Placenta
50	chr18:29466600-29477600	Strong transcription	Duodenum Mucosa	Duodenum

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